Canonical Allele Identifier: CA516373015

Gene: ZNF41

Linked Data

• MyVariant Identifiers: chrX:g.47308752T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.47449353T>C , CM000685.2:g.47449353T>C	GRCh38
NC_000023.10:g.47308752T>C , CM000685.1:g.47308752T>C	GRCh37
NC_000023.9:g.47193696T>C	NCBI36
NG_008238.1:g.38594A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000684689.1:c.417A>G MANE Select	ENSP00000508254.1:p.Gln139=
ENST00000313116.11:c.417A>G	ENSP00000315173.7:p.Gln139=
ENST00000377065.8:c.417A>G	ENSP00000366265.4:p.Gln139=
ENST00000432977.1:c.447A>G	ENSP00000390385.1:p.Gln149=
ENST00000465311.1:n.570A>G
NM_007130.2:c.417A>G	NP_009061.1:p.Gln139=
NM_153380.2:c.417A>G	NP_700359.1:p.Gln139=
XM_005272665.3:c.417A>G	XP_005272722.1:p.Gln139=
XM_005272666.3:c.417A>G	XP_005272723.1:p.Gln139=
XM_005272668.3:c.159A>G	XP_005272725.1:p.Gln53=
XM_005272669.3:c.159A>G	XP_005272726.1:p.Gln53=
XM_006724550.2:c.519A>G	XP_006724613.1:p.Gln173=
XM_006724554.2:c.447A>G	XP_006724617.1:p.Gln149=
XM_006724555.2:c.447A>G	XP_006724618.1:p.Gln149=
XM_006724556.2:c.423A>G	XP_006724619.1:p.Gln141=
XM_006724557.2:c.417A>G	XP_006724620.1:p.Gln139=
XM_006724558.2:c.159A>G	XP_006724621.1:p.Gln53=
XM_011543979.1:c.543A>G	XP_011542281.1:p.Gln181=
XM_011543980.1:c.543A>G	XP_011542282.1:p.Gln181=
XM_011543981.1:c.543A>G	XP_011542283.1:p.Gln181=
XM_011543982.1:c.159A>G	XP_011542284.1:p.Gln53=
NM_001324139.1:c.159A>G	NP_001311068.1:p.Gln53=
NM_001324140.1:c.417A>G	NP_001311069.1:p.Gln139=
NM_001324141.1:c.159A>G	NP_001311070.1:p.Gln53=
NM_001324142.1:c.423A>G	NP_001311071.1:p.Gln141=
NM_001324143.1:c.159A>G	NP_001311072.1:p.Gln53=
NM_001324144.1:c.417A>G	NP_001311073.1:p.Gln139=
NM_001324145.1:c.159A>G	NP_001311074.1:p.Gln53=
NM_001324147.1:c.417A>G	NP_001311076.1:p.Gln139=
NM_001324148.1:c.423A>G	NP_001311077.1:p.Gln141=
NM_001324149.1:c.159A>G	NP_001311078.1:p.Gln53=
NM_001324150.1:c.417A>G	NP_001311079.1:p.Gln139=
NM_001324151.1:c.447A>G	NP_001311080.1:p.Gln149=
NM_001324152.1:c.159A>G	NP_001311081.1:p.Gln53=
NM_001324153.1:c.447A>G	NP_001311082.1:p.Gln149=
NM_001324154.1:c.519A>G	NP_001311083.1:p.Gln173=
NM_001324155.1:c.543A>G	NP_001311084.1:p.Gln181=
NM_001324156.1:c.315A>G	NP_001311085.1:p.Gln105=
NM_001324157.1:c.309A>G	NP_001311086.1:p.Gln103=
NM_007130.3:c.417A>G	NP_009061.1:p.Gln139=
NM_153380.3:c.417A>G	NP_700359.1:p.Gln139=
XM_006724550.3:c.519A>G	XP_006724613.1:p.Gln173=
XM_006724555.3:c.447A>G	XP_006724618.1:p.Gln149=
XM_017029810.2:c.519A>G	XP_016885299.1:p.Gln173=
XM_017029811.2:c.519A>G	XP_016885300.1:p.Gln173=
XM_017029812.1:c.519A>G	XP_016885301.1:p.Gln173=
XM_017029813.1:c.519A>G	XP_016885302.1:p.Gln173=
XM_017029814.2:c.519A>G	XP_016885303.1:p.Gln173=
XM_017029815.1:c.519A>G	XP_016885304.1:p.Gln173=
XM_017029816.1:c.447A>G	XP_016885305.1:p.Gln149=
XM_017029817.1:c.417A>G	XP_016885306.1:p.Gln139=
NM_001324139.2:c.159A>G	NP_001311068.1:p.Gln53=
NM_001324140.2:c.417A>G	NP_001311069.1:p.Gln139=
NM_001324141.2:c.159A>G	NP_001311070.1:p.Gln53=
NM_001324142.2:c.423A>G	NP_001311071.1:p.Gln141=
NM_001324143.2:c.159A>G	NP_001311072.1:p.Gln53=
NM_001324144.2:c.417A>G MANE Select	NP_001311073.1:p.Gln139=
NM_001324145.2:c.159A>G	NP_001311074.1:p.Gln53=
NM_001324147.2:c.417A>G	NP_001311076.1:p.Gln139=
NM_001324148.2:c.423A>G	NP_001311077.1:p.Gln141=
NM_001324149.2:c.159A>G	NP_001311078.1:p.Gln53=
NM_001324150.2:c.417A>G	NP_001311079.1:p.Gln139=
NM_001324151.2:c.447A>G	NP_001311080.1:p.Gln149=
NM_001324152.2:c.159A>G	NP_001311081.1:p.Gln53=
NM_001324153.2:c.447A>G	NP_001311082.1:p.Gln149=
NM_007130.4:c.417A>G	NP_009061.1:p.Gln139=