Canonical Allele Identifier: CA605326247

Gene: TSPAN31

Linked Data

• dbSNP Id: rs778705354
• gnomAD v2: 12-58138892-C-A
• gnomAD v4: 12-57745109-C-A
• MyVariant Identifiers: chr12:g.58138892_58138893delinsAT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57745109C>A , CM000674.2:g.57745109C>A	GRCh38
NC_000012.11:g.58138892C>A , CM000674.1:g.58138892C>A	GRCh37
NC_000012.10:g.56425159C>A	NCBI36
NG_029755.1:g.2053G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000257910.8:c.-46C>A MANE Select	ENSP00000257910.3:n.-46C>A
ENST00000257910.7:c.-46C>A	ENSP00000257910.3:n.-46C>A
ENST00000546993.5:n.52C>A
ENST00000547311.5:n.236-636C>A
ENST00000547472.5:c.-46C>A	ENSP00000449199.1:n.-46C>A
ENST00000547992.5:c.-46C>A	ENSP00000448209.1:n.-46C>A
ENST00000548093.5:n.41C>A
ENST00000549052.5:c.-46C>A	ENSP00000450195.1:n.-46C>A
ENST00000550528.5:n.106-636C>A
ENST00000552816.5:c.-294C>A	ENSP00000449312.1:n.-294C>A
ENST00000553089.5:c.-46C>A	ENSP00000446482.1:n.-46C>A
ENST00000553221.5:n.250-636C>A
NM_005981.3:c.-46C>A	NP_005972.1:n.-46C>A
XM_005269074.2:c.211C>A	XP_005269131.2:p.Leu71Ile
NM_001330168.1:c.-46C>A	NP_001317097.1:n.-46C>A
NM_001330169.1:c.-294C>A	NP_001317098.1:n.-294C>A
NM_005981.4:c.-46C>A	NP_005972.1:n.-46C>A
NM_005981.5:c.-46C>A MANE Select	NP_005972.1:n.-46C>A
NM_001330168.2:c.-46C>A	NP_001317097.1:n.-46C>A
NM_001330169.2:c.-294C>A	NP_001317098.1:n.-294C>A