Canonical Allele Identifier: CA480294206

Gene: TSPAN31

Linked Data

• MyVariant Identifiers: chr12:g.58138982T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57745199T>G , CM000674.2:g.57745199T>G	GRCh38
NC_000012.11:g.58138982T>G , CM000674.1:g.58138982T>G	GRCh37
NC_000012.10:g.56425249T>G	NCBI36
NG_029755.1:g.1963A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000257910.8:c.45T>G MANE Select	ENSP00000257910.3:p.Ala15=
ENST00000257910.7:c.45T>G	ENSP00000257910.3:p.Ala15=
ENST00000546993.5:n.142T>G
ENST00000547311.5:n.236-546T>G
ENST00000547472.5:c.45T>G	ENSP00000449199.1:p.Ala15=
ENST00000547992.5:c.45T>G	ENSP00000448209.1:p.Ala15=
ENST00000548093.5:n.131T>G
ENST00000549052.5:c.45T>G	ENSP00000450195.1:p.Ala15=
ENST00000550528.5:n.106-546T>G
ENST00000552816.5:c.-204T>G	ENSP00000449312.1:n.-204T>G
ENST00000553089.5:c.45T>G	ENSP00000446482.1:p.Ala15=
ENST00000553221.5:n.250-546T>G
NM_005981.3:c.45T>G	NP_005972.1:p.Ala15=
XM_005269074.2:c.301T>G	XP_005269131.2:p.Ser101Ala
NM_001330168.1:c.45T>G	NP_001317097.1:p.Ala15=
NM_001330169.1:c.-204T>G	NP_001317098.1:n.-204T>G
NM_005981.4:c.45T>G	NP_005972.1:p.Ala15=
NM_005981.5:c.45T>G MANE Select	NP_005972.1:p.Ala15=
NM_001330168.2:c.45T>G	NP_001317097.1:p.Ala15=
NM_001330169.2:c.-204T>G	NP_001317098.1:n.-204T>G