Canonical Allele Identifier: CA2619496080

Gene: TSPAN31

Linked Data

• gnomAD v4: 12-57745105-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57745105T>C , CM000674.2:g.57745105T>C	GRCh38
NC_000012.11:g.58138888T>C , CM000674.1:g.58138888T>C	GRCh37
NC_000012.10:g.56425155T>C	NCBI36
NG_029755.1:g.2057A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000257910.8:c.-50T>C MANE Select	ENSP00000257910.3:n.-50T>C
ENST00000257910.7:c.-50T>C	ENSP00000257910.3:n.-50T>C
ENST00000546993.5:n.48T>C
ENST00000547311.5:n.236-640T>C
ENST00000547472.5:c.-50T>C	ENSP00000449199.1:n.-50T>C
ENST00000547992.5:c.-50T>C	ENSP00000448209.1:n.-50T>C
ENST00000548093.5:n.37T>C
ENST00000549052.5:c.-50T>C	ENSP00000450195.1:n.-50T>C
ENST00000550528.5:n.106-640T>C
ENST00000552816.5:c.-298T>C	ENSP00000449312.1:n.-298T>C
ENST00000553089.5:c.-50T>C	ENSP00000446482.1:n.-50T>C
ENST00000553221.5:n.250-640T>C
NM_005981.3:c.-50T>C	NP_005972.1:n.-50T>C
XM_005269074.2:c.207T>C	XP_005269131.2:p.Asn69=
NM_001330168.1:c.-50T>C	NP_001317097.1:n.-50T>C
NM_001330169.1:c.-298T>C	NP_001317098.1:n.-298T>C
NM_005981.4:c.-50T>C	NP_005972.1:n.-50T>C
NM_005981.5:c.-50T>C MANE Select	NP_005972.1:n.-50T>C
NM_001330168.2:c.-50T>C	NP_001317097.1:n.-50T>C
NM_001330169.2:c.-298T>C	NP_001317098.1:n.-298T>C