Canonical Allele Identifier: CA2659476119

Gene: TGFA

Linked Data

• gnomAD v4: 2-70450251-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70450251A>T , CM000664.2:g.70450251A>T	GRCh38
NC_000002.11:g.70677383A>T , CM000664.1:g.70677383A>T	GRCh37
NC_000002.10:g.70530891A>T	NCBI36
NG_029975.1:g.108765T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295400.11:c.*608T>A MANE Select	ENSP00000295400.6:n.*608T>A
ENST00000295400.10:c.*608T>A	ENSP00000295400.6:n.*608T>A
ENST00000418333.6:c.*608T>A	ENSP00000404099.2:n.*608T>A
ENST00000419940.5:c.379-630T>A
ENST00000445399.5:c.*19-630T>A	ENSP00000387493.1:n.*19-630T>A
NM_001099691.2:c.*608T>A	NP_001093161.1:n.*608T>A
NM_001308158.1:c.*608T>A	NP_001295087.1:n.*608T>A
NM_001308159.1:c.*608T>A	NP_001295088.1:n.*608T>A
NM_003236.3:c.*608T>A	NP_003227.1:n.*608T>A
NM_003236.4:c.*608T>A MANE Select	NP_003227.1:n.*608T>A
NM_001099691.3:c.*608T>A	NP_001093161.1:n.*608T>A
NM_001308158.2:c.*608T>A	NP_001295087.1:n.*608T>A
NM_001308159.2:c.*608T>A	NP_001295088.1:n.*608T>A