Canonical Allele Identifier: CA2039031054

Gene: TSPAN31

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57745192T= , CM000674.2:g.57745192T=	GRCh38
NC_000012.11:g.58138975T= , CM000674.1:g.58138975T=	GRCh37
NC_000012.10:g.56425242T=	NCBI36
NG_029755.1:g.1970A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000257910.8:c.38T= MANE Select	ENSP00000257910.3:p.Leu13=
ENST00000257910.7:c.38T=	ENSP00000257910.3:p.Leu13=
ENST00000546993.5:n.135T=
ENST00000547311.5:n.236-553T=
ENST00000547472.5:c.38T=	ENSP00000449199.1:p.Leu13=
ENST00000547992.5:c.38T=	ENSP00000448209.1:p.Leu13=
ENST00000548093.5:n.124T=
ENST00000549052.5:c.38T=	ENSP00000450195.1:p.Leu13=
ENST00000550528.5:n.106-553T=
ENST00000552816.5:c.-211T=	ENSP00000449312.1:n.-211T=
ENST00000553089.5:c.38T=	ENSP00000446482.1:p.Leu13=
ENST00000553221.5:n.250-553T=
NM_005981.3:c.38T=	NP_005972.1:p.Leu13=
XM_005269074.2:c.294T=	XP_005269131.2:p.Ala98=
NM_001330168.1:c.38T=	NP_001317097.1:p.Leu13=
NM_001330169.1:c.-211T=	NP_001317098.1:n.-211T=
NM_005981.4:c.38T=	NP_005972.1:p.Leu13=
NM_005981.5:c.38T= MANE Select	NP_005972.1:p.Leu13=
NM_001330168.2:c.38T=	NP_001317097.1:p.Leu13=
NM_001330169.2:c.-211T=	NP_001317098.1:n.-211T=