Canonical Allele Identifier: CA2659476117

Gene: TGFA

Linked Data

• gnomAD v4: 2-70450241-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70450241C>G , CM000664.2:g.70450241C>G	GRCh38
NC_000002.11:g.70677373C>G , CM000664.1:g.70677373C>G	GRCh37
NC_000002.10:g.70530881C>G	NCBI36
NG_029975.1:g.108775G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295400.11:c.*618G>C MANE Select	ENSP00000295400.6:n.*618G>C
ENST00000295400.10:c.*618G>C	ENSP00000295400.6:n.*618G>C
ENST00000418333.6:c.*618G>C	ENSP00000404099.2:n.*618G>C
ENST00000419940.5:c.379-620G>C
ENST00000445399.5:c.*19-620G>C	ENSP00000387493.1:n.*19-620G>C
NM_001099691.2:c.*618G>C	NP_001093161.1:n.*618G>C
NM_001308158.1:c.*618G>C	NP_001295087.1:n.*618G>C
NM_001308159.1:c.*618G>C	NP_001295088.1:n.*618G>C
NM_003236.3:c.*618G>C	NP_003227.1:n.*618G>C
NM_003236.4:c.*618G>C MANE Select	NP_003227.1:n.*618G>C
NM_001099691.3:c.*618G>C	NP_001093161.1:n.*618G>C
NM_001308158.2:c.*618G>C	NP_001295087.1:n.*618G>C
NM_001308159.2:c.*618G>C	NP_001295088.1:n.*618G>C