Canonical Allele Identifier: CA2575206078

Gene: TSPAN31

Linked Data

• gnomAD v4: 12-57745095-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57745095C>T , CM000674.2:g.57745095C>T	GRCh38
NC_000012.11:g.58138878C>T , CM000674.1:g.58138878C>T	GRCh37
NC_000012.10:g.56425145C>T	NCBI36
NG_029755.1:g.2067G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000257910.8:c.-60C>T MANE Select	ENSP00000257910.3:n.-60C>T
ENST00000257910.7:c.-60C>T	ENSP00000257910.3:n.-60C>T
ENST00000546993.5:n.38C>T
ENST00000547311.5:n.236-650C>T
ENST00000547472.5:c.-60C>T	ENSP00000449199.1:n.-60C>T
ENST00000547992.5:c.-60C>T	ENSP00000448209.1:n.-60C>T
ENST00000548093.5:n.27C>T
ENST00000549052.5:c.-60C>T	ENSP00000450195.1:n.-60C>T
ENST00000550528.5:n.106-650C>T
ENST00000552816.5:c.-308C>T	ENSP00000449312.1:n.-308C>T
ENST00000553089.5:c.-60C>T	ENSP00000446482.1:n.-60C>T
ENST00000553221.5:n.250-650C>T
NM_005981.3:c.-60C>T	NP_005972.1:n.-60C>T
XM_005269074.2:c.197C>T	XP_005269131.2:p.Thr66Met
NM_001330168.1:c.-60C>T	NP_001317097.1:n.-60C>T
NM_001330169.1:c.-308C>T	NP_001317098.1:n.-308C>T
NM_005981.4:c.-60C>T	NP_005972.1:n.-60C>T
NM_005981.5:c.-60C>T MANE Select	NP_005972.1:n.-60C>T
NM_001330168.2:c.-60C>T	NP_001317097.1:n.-60C>T
NM_001330169.2:c.-308C>T	NP_001317098.1:n.-308C>T