Canonical Allele Identifier: CA385535535

Gene: TSPAN31

Linked Data

• dbSNP Id: rs1230296837
• gnomAD v2: 12-58138972-C-T
• gnomAD v4: 12-57745189-C-T
• MyVariant Identifiers: chr12:g.58138972C>T (hg19) ; chr12:g.57745189C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57745189C>T , CM000674.2:g.57745189C>T	GRCh38
NC_000012.11:g.58138972C>T , CM000674.1:g.58138972C>T	GRCh37
NC_000012.10:g.56425239C>T	NCBI36
NG_029755.1:g.1973G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000257910.8:c.35C>T MANE Select	ENSP00000257910.3:p.Ala12Val
ENST00000257910.7:c.35C>T	ENSP00000257910.3:p.Ala12Val
ENST00000546993.5:n.132C>T
ENST00000547311.5:n.236-556C>T
ENST00000547472.5:c.35C>T	ENSP00000449199.1:p.Ala12Val
ENST00000547992.5:c.35C>T	ENSP00000448209.1:p.Ala12Val
ENST00000548093.5:n.121C>T
ENST00000549052.5:c.35C>T	ENSP00000450195.1:p.Ala12Val
ENST00000550528.5:n.106-556C>T
ENST00000552816.5:c.-214C>T	ENSP00000449312.1:n.-214C>T
ENST00000553089.5:c.35C>T	ENSP00000446482.1:p.Ala12Val
ENST00000553221.5:n.250-556C>T
NM_005981.3:c.35C>T	NP_005972.1:p.Ala12Val
XM_005269074.2:c.291C>T	XP_005269131.2:p.Cys97=
NM_001330168.1:c.35C>T	NP_001317097.1:p.Ala12Val
NM_001330169.1:c.-214C>T	NP_001317098.1:n.-214C>T
NM_005981.4:c.35C>T	NP_005972.1:p.Ala12Val
NM_005981.5:c.35C>T MANE Select	NP_005972.1:p.Ala12Val
NM_001330168.2:c.35C>T	NP_001317097.1:p.Ala12Val
NM_001330169.2:c.-214C>T	NP_001317098.1:n.-214C>T