Canonical Allele Identifier: CA355537590

Gene: SPATA16

Linked Data

• MyVariant Identifiers: chr3:g.172737295T>A (hg19) ; chr3:g.173019505T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.173019505T>A , CM000665.2:g.173019505T>A	GRCh38
NC_000003.11:g.172737295T>A , CM000665.1:g.172737295T>A	GRCh37
NC_000003.10:g.174219989T>A	NCBI36
NG_021422.1:g.126764A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351008.4:c.829A>T MANE Select	ENSP00000341765.3:p.Arg277Trp
ENST00000351008.3:c.829A>T	ENSP00000341765.3:p.Arg277Trp
NM_031955.5:c.829A>T	NP_114161.3:p.Arg277Trp
XM_006713778.2:c.829A>T	XP_006713841.1:p.Arg277Trp
XM_011513222.1:c.829A>T	XP_011511524.1:p.Arg277Trp
XM_006713778.3:c.829A>T	XP_006713841.1:p.Arg277Trp
XM_017007308.2:c.829A>T	XP_016862797.1:p.Arg277Trp
NM_031955.6:c.829A>T MANE Select	NP_114161.3:p.Arg277Trp