Canonical Allele Identifier: CA2659476183

Gene: TGFA

Linked Data

• gnomAD v4: 2-70450315-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70450315T>G , CM000664.2:g.70450315T>G	GRCh38
NC_000002.11:g.70677447T>G , CM000664.1:g.70677447T>G	GRCh37
NC_000002.10:g.70530955T>G	NCBI36
NG_029975.1:g.108701A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000295400.11:c.*544A>C MANE Select	ENSP00000295400.6:n.*544A>C
ENST00000295400.10:c.*544A>C	ENSP00000295400.6:n.*544A>C
ENST00000418333.6:c.*544A>C	ENSP00000404099.2:n.*544A>C
ENST00000419940.5:c.379-694A>C
ENST00000445399.5:c.*19-694A>C	ENSP00000387493.1:n.*19-694A>C
NM_001099691.2:c.*544A>C	NP_001093161.1:n.*544A>C
NM_001308158.1:c.*544A>C	NP_001295087.1:n.*544A>C
NM_001308159.1:c.*544A>C	NP_001295088.1:n.*544A>C
NM_003236.3:c.*544A>C	NP_003227.1:n.*544A>C
NM_003236.4:c.*544A>C MANE Select	NP_003227.1:n.*544A>C
NM_001099691.3:c.*544A>C	NP_001093161.1:n.*544A>C
NM_001308158.2:c.*544A>C	NP_001295087.1:n.*544A>C
NM_001308159.2:c.*544A>C	NP_001295088.1:n.*544A>C