Canonical Allele Identifier: CA2668589007

Gene: SPATA16

Linked Data

• gnomAD v4: 3-173019389-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.173019389G>C , CM000665.2:g.173019389G>C	GRCh38
NC_000003.11:g.172737179G>C , CM000665.1:g.172737179G>C	GRCh37
NC_000003.10:g.174219873G>C	NCBI36
NG_021422.1:g.126880C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000351008.4:c.848+97C>G MANE Select	ENSP00000341765.3:n.848+97C>G
ENST00000351008.3:c.848+97C>G	ENSP00000341765.3:n.848+97C>G
NM_031955.5:c.848+97C>G	NP_114161.3:n.848+97C>G
XM_006713778.2:c.848+97C>G	XP_006713841.1:n.848+97C>G
XM_011513222.1:c.848+97C>G	XP_011511524.1:n.848+97C>G
XM_006713778.3:c.848+97C>G	XP_006713841.1:n.848+97C>G
XM_017007308.2:c.848+97C>G	XP_016862797.1:n.848+97C>G
NM_031955.6:c.848+97C>G MANE Select	NP_114161.3:n.848+97C>G