Canonical Allele Identifier: CA1420814327

Gene: SPATA16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.173125487T= , CM000665.2:g.173125487T=	GRCh38
NC_000003.11:g.172843277T= , CM000665.1:g.172843277T=	GRCh37
NC_000003.10:g.174325971T=	NCBI36
NG_021422.1:g.20782A=

Transcript Alleles

HGVS	Amino-acid Change
NM_031955.6:c.-18-7738A= MANE Select	NP_114161.3:n.-18-7738A=
ENST00000351008.4:c.-18-7738A= MANE Select	ENSP00000341765.3:n.-18-7738A=
NM_031955.5:c.-18-7738A=	NP_114161.3:n.-18-7738A=
ENST00000351008.3:c.-18-7738A=	ENSP00000341765.3:n.-18-7738A=
XM_006713778.2:c.-18-7738A=	XP_006713841.1:n.-18-7738A=
XM_006713778.3:c.-18-7738A=	XP_006713841.1:n.-18-7738A=
XM_011513222.1:c.-18-7738A=	XP_011511524.1:n.-18-7738A=
XM_017007308.2:c.-18-7738A=	XP_016862797.1:n.-18-7738A=
XR_001741021.1:n.65+11135T=
XR_924722.1:n.133+11135T=