Canonical Allele Identifier: CA2619496079

Gene: TSPAN31

Linked Data

• gnomAD v4: 12-57745103-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57745103A>G , CM000674.2:g.57745103A>G	GRCh38
NC_000012.11:g.58138886A>G , CM000674.1:g.58138886A>G	GRCh37
NC_000012.10:g.56425153A>G	NCBI36
NG_029755.1:g.2059T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000257910.8:c.-52A>G MANE Select	ENSP00000257910.3:n.-52A>G
ENST00000257910.7:c.-52A>G	ENSP00000257910.3:n.-52A>G
ENST00000546993.5:n.46A>G
ENST00000547311.5:n.236-642A>G
ENST00000547472.5:c.-52A>G	ENSP00000449199.1:n.-52A>G
ENST00000547992.5:c.-52A>G	ENSP00000448209.1:n.-52A>G
ENST00000548093.5:n.35A>G
ENST00000549052.5:c.-52A>G	ENSP00000450195.1:n.-52A>G
ENST00000550528.5:n.106-642A>G
ENST00000552816.5:c.-300A>G	ENSP00000449312.1:n.-300A>G
ENST00000553089.5:c.-52A>G	ENSP00000446482.1:n.-52A>G
ENST00000553221.5:n.250-642A>G
NM_005981.3:c.-52A>G	NP_005972.1:n.-52A>G
XM_005269074.2:c.205A>G	XP_005269131.2:p.Asn69Asp
NM_001330168.1:c.-52A>G	NP_001317097.1:n.-52A>G
NM_001330169.1:c.-300A>G	NP_001317098.1:n.-300A>G
NM_005981.4:c.-52A>G	NP_005972.1:n.-52A>G
NM_005981.5:c.-52A>G MANE Select	NP_005972.1:n.-52A>G
NM_001330168.2:c.-52A>G	NP_001317097.1:n.-52A>G
NM_001330169.2:c.-300A>G	NP_001317098.1:n.-300A>G