Canonical Allele Identifier: CA2039031065

Gene: TSPAN31

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57745197G= , CM000674.2:g.57745197G=	GRCh38
NC_000012.11:g.58138980G= , CM000674.1:g.58138980G=	GRCh37
NC_000012.10:g.56425247G=	NCBI36
NG_029755.1:g.1965C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000257910.8:c.43G= MANE Select	ENSP00000257910.3:p.Ala15=
ENST00000257910.7:c.43G=	ENSP00000257910.3:p.Ala15=
ENST00000546993.5:n.140G=
ENST00000547311.5:n.236-548G=
ENST00000547472.5:c.43G=	ENSP00000449199.1:p.Ala15=
ENST00000547992.5:c.43G=	ENSP00000448209.1:p.Ala15=
ENST00000548093.5:n.129G=
ENST00000549052.5:c.43G=	ENSP00000450195.1:p.Ala15=
ENST00000550528.5:n.106-548G=
ENST00000552816.5:c.-206G=	ENSP00000449312.1:n.-206G=
ENST00000553089.5:c.43G=	ENSP00000446482.1:p.Ala15=
ENST00000553221.5:n.250-548G=
NM_005981.3:c.43G=	NP_005972.1:p.Ala15=
XM_005269074.2:c.299G=	XP_005269131.2:p.Arg100=
NM_001330168.1:c.43G=	NP_001317097.1:p.Ala15=
NM_001330169.1:c.-206G=	NP_001317098.1:n.-206G=
NM_005981.4:c.43G=	NP_005972.1:p.Ala15=
NM_005981.5:c.43G= MANE Select	NP_005972.1:p.Ala15=
NM_001330168.2:c.43G=	NP_001317097.1:p.Ala15=
NM_001330169.2:c.-206G=	NP_001317098.1:n.-206G=