Canonical Allele Identifier: CA329720557

Gene: ZNF41

Linked Data

• dbSNP Id: rs1043232505
• gnomAD v3: X-47449520-G-T
• gnomAD v4: X-47449520-G-T
• MyVariant Identifiers: chrX:g.47308919G>T (hg19) ; chrX:g.47449520G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47449520G>T , CM000685.2:g.47449520G>T	GRCh38
NC_000023.10:g.47308919G>T , CM000685.1:g.47308919G>T	GRCh37
NC_000023.9:g.47193863G>T	NCBI36
NG_008238.1:g.38427C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684689.1:c.296-46C>A MANE Select	ENSP00000508254.1:n.296-46C>A
ENST00000313116.11:c.296-46C>A	ENSP00000315173.7:n.296-46C>A
ENST00000377065.8:c.296-46C>A	ENSP00000366265.4:n.296-46C>A
ENST00000432977.1:c.326-46C>A	ENSP00000390385.1:n.326-46C>A
ENST00000465311.1:n.449-46C>A
NM_007130.2:c.296-46C>A	NP_009061.1:n.296-46C>A
NM_153380.2:c.296-46C>A	NP_700359.1:n.296-46C>A
XM_005272665.3:c.296-46C>A	XP_005272722.1:n.296-46C>A
XM_005272666.3:c.296-46C>A	XP_005272723.1:n.296-46C>A
XM_005272668.3:c.38-46C>A	XP_005272725.1:n.38-46C>A
XM_005272669.3:c.38-46C>A	XP_005272726.1:n.38-46C>A
XM_006724550.2:c.398-46C>A	XP_006724613.1:n.398-46C>A
XM_006724554.2:c.326-46C>A	XP_006724617.1:n.326-46C>A
XM_006724555.2:c.326-46C>A	XP_006724618.1:n.326-46C>A
XM_006724556.2:c.302-46C>A	XP_006724619.1:n.302-46C>A
XM_006724557.2:c.296-46C>A	XP_006724620.1:n.296-46C>A
XM_006724558.2:c.38-46C>A	XP_006724621.1:n.38-46C>A
XM_011543979.1:c.422-46C>A	XP_011542281.1:n.422-46C>A
XM_011543980.1:c.422-46C>A	XP_011542282.1:n.422-46C>A
XM_011543981.1:c.422-46C>A	XP_011542283.1:n.422-46C>A
XM_011543982.1:c.38-46C>A	XP_011542284.1:n.38-46C>A
NM_001324139.1:c.38-46C>A	NP_001311068.1:n.38-46C>A
NM_001324140.1:c.296-46C>A	NP_001311069.1:n.296-46C>A
NM_001324141.1:c.38-46C>A	NP_001311070.1:n.38-46C>A
NM_001324142.1:c.302-46C>A	NP_001311071.1:n.302-46C>A
NM_001324143.1:c.38-46C>A	NP_001311072.1:n.38-46C>A
NM_001324144.1:c.296-46C>A	NP_001311073.1:n.296-46C>A
NM_001324145.1:c.38-46C>A	NP_001311074.1:n.38-46C>A
NM_001324147.1:c.296-46C>A	NP_001311076.1:n.296-46C>A
NM_001324148.1:c.302-46C>A	NP_001311077.1:n.302-46C>A
NM_001324149.1:c.38-46C>A	NP_001311078.1:n.38-46C>A
NM_001324150.1:c.296-46C>A	NP_001311079.1:n.296-46C>A
NM_001324151.1:c.326-46C>A	NP_001311080.1:n.326-46C>A
NM_001324152.1:c.38-46C>A	NP_001311081.1:n.38-46C>A
NM_001324153.1:c.326-46C>A	NP_001311082.1:n.326-46C>A
NM_001324154.1:c.398-46C>A	NP_001311083.1:n.398-46C>A
NM_001324155.1:c.422-46C>A	NP_001311084.1:n.422-46C>A
NM_001324156.1:c.302-154C>A	NP_001311085.1:n.302-154C>A
NM_001324157.1:c.296-154C>A	NP_001311086.1:n.296-154C>A
NM_007130.3:c.296-46C>A	NP_009061.1:n.296-46C>A
NM_153380.3:c.296-46C>A	NP_700359.1:n.296-46C>A
XM_006724550.3:c.398-46C>A	XP_006724613.1:n.398-46C>A
XM_006724555.3:c.326-46C>A	XP_006724618.1:n.326-46C>A
XM_017029810.2:c.398-46C>A	XP_016885299.1:n.398-46C>A
XM_017029811.2:c.398-46C>A	XP_016885300.1:n.398-46C>A
XM_017029812.1:c.398-46C>A	XP_016885301.1:n.398-46C>A
XM_017029813.1:c.398-46C>A	XP_016885302.1:n.398-46C>A
XM_017029814.2:c.398-46C>A	XP_016885303.1:n.398-46C>A
XM_017029815.1:c.398-46C>A	XP_016885304.1:n.398-46C>A
XM_017029816.1:c.326-46C>A	XP_016885305.1:n.326-46C>A
XM_017029817.1:c.296-46C>A	XP_016885306.1:n.296-46C>A
NM_001324139.2:c.38-46C>A	NP_001311068.1:n.38-46C>A
NM_001324140.2:c.296-46C>A	NP_001311069.1:n.296-46C>A
NM_001324141.2:c.38-46C>A	NP_001311070.1:n.38-46C>A
NM_001324142.2:c.302-46C>A	NP_001311071.1:n.302-46C>A
NM_001324143.2:c.38-46C>A	NP_001311072.1:n.38-46C>A
NM_001324144.2:c.296-46C>A MANE Select	NP_001311073.1:n.296-46C>A
NM_001324145.2:c.38-46C>A	NP_001311074.1:n.38-46C>A
NM_001324147.2:c.296-46C>A	NP_001311076.1:n.296-46C>A
NM_001324148.2:c.302-46C>A	NP_001311077.1:n.302-46C>A
NM_001324149.2:c.38-46C>A	NP_001311078.1:n.38-46C>A
NM_001324150.2:c.296-46C>A	NP_001311079.1:n.296-46C>A
NM_001324151.2:c.326-46C>A	NP_001311080.1:n.326-46C>A
NM_001324152.2:c.38-46C>A	NP_001311081.1:n.38-46C>A
NM_001324153.2:c.326-46C>A	NP_001311082.1:n.326-46C>A
NM_007130.4:c.296-46C>A	NP_009061.1:n.296-46C>A