Canonical Allele Identifier: CA2659476121

Gene: TGFA

Linked Data

• gnomAD v4: 2-70450257-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70450257C>A , CM000664.2:g.70450257C>A	GRCh38
NC_000002.11:g.70677389C>A , CM000664.1:g.70677389C>A	GRCh37
NC_000002.10:g.70530897C>A	NCBI36
NG_029975.1:g.108759G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000295400.11:c.*602G>T MANE Select	ENSP00000295400.6:n.*602G>T
ENST00000295400.10:c.*602G>T	ENSP00000295400.6:n.*602G>T
ENST00000418333.6:c.*602G>T	ENSP00000404099.2:n.*602G>T
ENST00000419940.5:c.379-636G>T
ENST00000445399.5:c.*19-636G>T	ENSP00000387493.1:n.*19-636G>T
NM_001099691.2:c.*602G>T	NP_001093161.1:n.*602G>T
NM_001308158.1:c.*602G>T	NP_001295087.1:n.*602G>T
NM_001308159.1:c.*602G>T	NP_001295088.1:n.*602G>T
NM_003236.3:c.*602G>T	NP_003227.1:n.*602G>T
NM_003236.4:c.*602G>T MANE Select	NP_003227.1:n.*602G>T
NM_001099691.3:c.*602G>T	NP_001093161.1:n.*602G>T
NM_001308158.2:c.*602G>T	NP_001295087.1:n.*602G>T
NM_001308159.2:c.*602G>T	NP_001295088.1:n.*602G>T