Canonical Allele Identifier: CA385535604

Gene: TSPAN31

Linked Data

• MyVariant Identifiers: chr12:g.58138983C>G (hg19) ; chr12:g.57745200C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57745200C>G , CM000674.2:g.57745200C>G	GRCh38
NC_000012.11:g.58138983C>G , CM000674.1:g.58138983C>G	GRCh37
NC_000012.10:g.56425250C>G	NCBI36
NG_029755.1:g.1962G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000257910.8:c.46C>G MANE Select	ENSP00000257910.3:p.Leu16Val
ENST00000257910.7:c.46C>G	ENSP00000257910.3:p.Leu16Val
ENST00000546993.5:n.143C>G
ENST00000547311.5:n.236-545C>G
ENST00000547472.5:c.46C>G	ENSP00000449199.1:p.Leu16Val
ENST00000547992.5:c.46C>G	ENSP00000448209.1:p.Leu16Val
ENST00000548093.5:n.132C>G
ENST00000549052.5:c.46C>G	ENSP00000450195.1:p.Leu16Val
ENST00000550528.5:n.106-545C>G
ENST00000552816.5:c.-203C>G	ENSP00000449312.1:n.-203C>G
ENST00000553089.5:c.46C>G	ENSP00000446482.1:p.Leu16Val
ENST00000553221.5:n.250-545C>G
NM_005981.3:c.46C>G	NP_005972.1:p.Leu16Val
XM_005269074.2:c.302C>G	XP_005269131.2:p.Ser101Cys
NM_001330168.1:c.46C>G	NP_001317097.1:p.Leu16Val
NM_001330169.1:c.-203C>G	NP_001317098.1:n.-203C>G
NM_005981.4:c.46C>G	NP_005972.1:p.Leu16Val
NM_005981.5:c.46C>G MANE Select	NP_005972.1:p.Leu16Val
NM_001330168.2:c.46C>G	NP_001317097.1:p.Leu16Val
NM_001330169.2:c.-203C>G	NP_001317098.1:n.-203C>G