Canonical Allele Identifier: CA2039030931

Gene: TSPAN31

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57745094A= , CM000674.2:g.57745094A=	GRCh38
NC_000012.11:g.58138877A= , CM000674.1:g.58138877A=	GRCh37
NC_000012.10:g.56425144A=	NCBI36
NG_029755.1:g.2068T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000257910.8:c.-61A= MANE Select	ENSP00000257910.3:n.-61A=
ENST00000257910.7:c.-61A=	ENSP00000257910.3:n.-61A=
ENST00000546993.5:n.37A=
ENST00000547311.5:n.236-651A=
ENST00000547472.5:c.-61A=	ENSP00000449199.1:n.-61A=
ENST00000547992.5:c.-61A=	ENSP00000448209.1:n.-61A=
ENST00000548093.5:n.26A=
ENST00000549052.5:c.-61A=	ENSP00000450195.1:n.-61A=
ENST00000550528.5:n.106-651A=
ENST00000552816.5:c.-309A=	ENSP00000449312.1:n.-309A=
ENST00000553089.5:c.-61A=	ENSP00000446482.1:n.-61A=
ENST00000553221.5:n.250-651A=
NM_005981.3:c.-61A=	NP_005972.1:n.-61A=
XM_005269074.2:c.196A=	XP_005269131.2:p.Thr66=
NM_001330168.1:c.-61A=	NP_001317097.1:n.-61A=
NM_001330169.1:c.-309A=	NP_001317098.1:n.-309A=
NM_005981.4:c.-61A=	NP_005972.1:n.-61A=
NM_005981.5:c.-61A= MANE Select	NP_005972.1:n.-61A=
NM_001330168.2:c.-61A=	NP_001317097.1:n.-61A=
NM_001330169.2:c.-309A=	NP_001317098.1:n.-309A=