Canonical Allele Identifier: CA2039030952

Gene: TSPAN31

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57745109_57745110delinsCT , CM000674.2:g.57745109_57745110delinsCT	GRCh38
NC_000012.11:g.58138892_58138893delinsCT , CM000674.1:g.58138892_58138893delinsCT	GRCh37
NC_000012.10:g.56425159_56425160delinsCT	NCBI36
NG_029755.1:g.2052_2053delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000257910.8:c.-46_-45delinsCT MANE Select	ENSP00000257910.3:n.-46_-45delinsCT
ENST00000257910.7:c.-46_-45delinsCT	ENSP00000257910.3:n.-46_-45delinsCT
ENST00000546993.5:n.52_53delinsCT
ENST00000547311.5:n.236-636_236-635delinsCT
ENST00000547472.5:c.-46_-45delinsCT	ENSP00000449199.1:n.-46_-45delinsCT
ENST00000547992.5:c.-46_-45delinsCT	ENSP00000448209.1:n.-46_-45delinsCT
ENST00000548093.5:n.41_42delinsCT
ENST00000549052.5:c.-46_-45delinsCT	ENSP00000450195.1:n.-46_-45delinsCT
ENST00000550528.5:n.106-636_106-635delinsCT
ENST00000552816.5:c.-294_-293delinsCT	ENSP00000449312.1:n.-294_-293delinsCT
ENST00000553089.5:c.-46_-45delinsCT	ENSP00000446482.1:n.-46_-45delinsCT
ENST00000553221.5:n.250-636_250-635delinsCT
NM_005981.3:c.-46_-45delinsCT	NP_005972.1:n.-46_-45delinsCT
XM_005269074.2:c.211_212delinsCT	XP_005269131.2:p.Leu71=
NM_001330168.1:c.-46_-45delinsCT	NP_001317097.1:n.-46_-45delinsCT
NM_001330169.1:c.-294_-293delinsCT	NP_001317098.1:n.-294_-293delinsCT
NM_005981.4:c.-46_-45delinsCT	NP_005972.1:n.-46_-45delinsCT
NM_005981.5:c.-46_-45delinsCT MANE Select	NP_005972.1:n.-46_-45delinsCT
NM_001330168.2:c.-46_-45delinsCT	NP_001317097.1:n.-46_-45delinsCT
NM_001330169.2:c.-294_-293delinsCT	NP_001317098.1:n.-294_-293delinsCT