Canonical Allele Identifier: CA641905674

Gene: ZNF41

Linked Data

• dbSNP Id: rs1569275279
• gnomAD v2: X-47308760-GTTC-G
• gnomAD v4: X-47449361-GTTC-G
• MyVariant Identifiers: chrX:g.47308761_47308763del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47449366_47449368del , CM000685.2:g.47449366_47449368del	GRCh38
NC_000023.10:g.47308765_47308767del , CM000685.1:g.47308765_47308767del	GRCh37
NC_000023.9:g.47193709_47193711del	NCBI36
NG_008238.1:g.38583_38585del

Transcript Alleles

HGVS	Amino-acid change
ENST00000684689.1:c.406_408del MANE Select	ENSP00000508254.1:p.Glu136del
ENST00000313116.11:c.406_408del	ENSP00000315173.7:p.Glu136del
ENST00000377065.8:c.406_408del	ENSP00000366265.4:p.Glu136del
ENST00000432977.1:c.436_438del	ENSP00000390385.1:p.Glu146del
ENST00000465311.1:n.559_561del
NM_007130.2:c.406_408del	NP_009061.1:p.Glu136del
NM_153380.2:c.406_408del	NP_700359.1:p.Glu136del
XM_005272665.3:c.406_408del	XP_005272722.1:p.Glu136del
XM_005272666.3:c.406_408del	XP_005272723.1:p.Glu136del
XM_005272668.3:c.148_150del	XP_005272725.1:p.Glu50del
XM_005272669.3:c.148_150del	XP_005272726.1:p.Glu50del
XM_006724550.2:c.508_510del	XP_006724613.1:p.Glu170del
XM_006724554.2:c.436_438del	XP_006724617.1:p.Glu146del
XM_006724555.2:c.436_438del	XP_006724618.1:p.Glu146del
XM_006724556.2:c.412_414del	XP_006724619.1:p.Glu138del
XM_006724557.2:c.406_408del	XP_006724620.1:p.Glu136del
XM_006724558.2:c.148_150del	XP_006724621.1:p.Glu50del
XM_011543979.1:c.532_534del	XP_011542281.1:p.Glu178del
XM_011543980.1:c.532_534del	XP_011542282.1:p.Glu178del
XM_011543981.1:c.532_534del	XP_011542283.1:p.Glu178del
XM_011543982.1:c.148_150del	XP_011542284.1:p.Glu50del
NM_001324139.1:c.148_150del	NP_001311068.1:p.Glu50del
NM_001324140.1:c.406_408del	NP_001311069.1:p.Glu136del
NM_001324141.1:c.148_150del	NP_001311070.1:p.Glu50del
NM_001324142.1:c.412_414del	NP_001311071.1:p.Glu138del
NM_001324143.1:c.148_150del	NP_001311072.1:p.Glu50del
NM_001324144.1:c.406_408del	NP_001311073.1:p.Glu136del
NM_001324145.1:c.148_150del	NP_001311074.1:p.Glu50del
NM_001324147.1:c.406_408del	NP_001311076.1:p.Glu136del
NM_001324148.1:c.412_414del	NP_001311077.1:p.Glu138del
NM_001324149.1:c.148_150del	NP_001311078.1:p.Glu50del
NM_001324150.1:c.406_408del	NP_001311079.1:p.Glu136del
NM_001324151.1:c.436_438del	NP_001311080.1:p.Glu146del
NM_001324152.1:c.148_150del	NP_001311081.1:p.Glu50del
NM_001324153.1:c.436_438del	NP_001311082.1:p.Glu146del
NM_001324154.1:c.508_510del	NP_001311083.1:p.Glu170del
NM_001324155.1:c.532_534del	NP_001311084.1:p.Glu178del
NM_001324156.1:c.304_306del
NM_001324157.1:c.298_300del
NM_007130.3:c.406_408del	NP_009061.1:p.Glu136del
NM_153380.3:c.406_408del	NP_700359.1:p.Glu136del
XM_006724550.3:c.508_510del	XP_006724613.1:p.Glu170del
XM_006724555.3:c.436_438del	XP_006724618.1:p.Glu146del
XM_017029810.2:c.508_510del	XP_016885299.1:p.Glu170del
XM_017029811.2:c.508_510del	XP_016885300.1:p.Glu170del
XM_017029812.1:c.508_510del	XP_016885301.1:p.Glu170del
XM_017029813.1:c.508_510del	XP_016885302.1:p.Glu170del
XM_017029814.2:c.508_510del	XP_016885303.1:p.Glu170del
XM_017029815.1:c.508_510del	XP_016885304.1:p.Glu170del
XM_017029816.1:c.436_438del	XP_016885305.1:p.Glu146del
XM_017029817.1:c.406_408del	XP_016885306.1:p.Glu136del
NM_001324139.2:c.148_150del	NP_001311068.1:p.Glu50del
NM_001324140.2:c.406_408del	NP_001311069.1:p.Glu136del
NM_001324141.2:c.148_150del	NP_001311070.1:p.Glu50del
NM_001324142.2:c.412_414del	NP_001311071.1:p.Glu138del
NM_001324143.2:c.148_150del	NP_001311072.1:p.Glu50del
NM_001324144.2:c.406_408del MANE Select	NP_001311073.1:p.Glu136del
NM_001324145.2:c.148_150del	NP_001311074.1:p.Glu50del
NM_001324147.2:c.406_408del	NP_001311076.1:p.Glu136del
NM_001324148.2:c.412_414del	NP_001311077.1:p.Glu138del
NM_001324149.2:c.148_150del	NP_001311078.1:p.Glu50del
NM_001324150.2:c.406_408del	NP_001311079.1:p.Glu136del
NM_001324151.2:c.436_438del	NP_001311080.1:p.Glu146del
NM_001324152.2:c.148_150del	NP_001311081.1:p.Glu50del
NM_001324153.2:c.436_438del	NP_001311082.1:p.Glu146del
NM_007130.4:c.406_408del	NP_009061.1:p.Glu136del