Canonical Allele Identifier: CA2708337

Gene: SPATA16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.173117242G>A , CM000665.2:g.173117242G>A	GRCh38
NC_000003.11:g.172835032G>A , CM000665.1:g.172835032G>A	GRCh37
NC_000003.10:g.174317726G>A	NCBI36
NG_021422.1:g.29027C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_031955.6:c.490C>T MANE Select	NP_114161.3:p.His164Tyr
ENST00000351008.4:c.490C>T MANE Select	ENSP00000341765.3:p.His164Tyr
NM_031955.5:c.490C>T	NP_114161.3:p.His164Tyr
ENST00000351008.3:c.490C>T	ENSP00000341765.3:p.His164Tyr
XM_006713778.2:c.490C>T	XP_006713841.1:p.His164Tyr
XM_006713778.3:c.490C>T	XP_006713841.1:p.His164Tyr
XM_011513222.1:c.490C>T	XP_011511524.1:p.His164Tyr
XM_017007308.2:c.490C>T	XP_016862797.1:p.His164Tyr
XR_001741021.1:n.65+2890G>A
XR_924722.1:n.133+2890G>A
XR_924723.1:n.134-1077G>A