Canonical Allele Identifier: CA385535579

Gene: TSPAN31

Linked Data

• MyVariant Identifiers: chr12:g.58138979C>G (hg19) ; chr12:g.57745196C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57745196C>G , CM000674.2:g.57745196C>G	GRCh38
NC_000012.11:g.58138979C>G , CM000674.1:g.58138979C>G	GRCh37
NC_000012.10:g.56425246C>G	NCBI36
NG_029755.1:g.1966G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000257910.8:c.42C>G MANE Select	ENSP00000257910.3:p.Cys14Trp
ENST00000257910.7:c.42C>G	ENSP00000257910.3:p.Cys14Trp
ENST00000546993.5:n.139C>G
ENST00000547311.5:n.236-549C>G
ENST00000547472.5:c.42C>G	ENSP00000449199.1:p.Cys14Trp
ENST00000547992.5:c.42C>G	ENSP00000448209.1:p.Cys14Trp
ENST00000548093.5:n.128C>G
ENST00000549052.5:c.42C>G	ENSP00000450195.1:p.Cys14Trp
ENST00000550528.5:n.106-549C>G
ENST00000552816.5:c.-207C>G	ENSP00000449312.1:n.-207C>G
ENST00000553089.5:c.42C>G	ENSP00000446482.1:p.Cys14Trp
ENST00000553221.5:n.250-549C>G
NM_005981.3:c.42C>G	NP_005972.1:p.Cys14Trp
XM_005269074.2:c.298C>G	XP_005269131.2:p.Arg100Gly
NM_001330168.1:c.42C>G	NP_001317097.1:p.Cys14Trp
NM_001330169.1:c.-207C>G	NP_001317098.1:n.-207C>G
NM_005981.4:c.42C>G	NP_005972.1:p.Cys14Trp
NM_005981.5:c.42C>G MANE Select	NP_005972.1:p.Cys14Trp
NM_001330168.2:c.42C>G	NP_001317097.1:p.Cys14Trp
NM_001330169.2:c.-207C>G	NP_001317098.1:n.-207C>G