Canonical Allele Identifier: CA1259573936
Gene: TGFA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70450212A= , CM000664.2:g.70450212A= GRCh38
NC_000002.11:g.70677344A= , CM000664.1:g.70677344A= GRCh37
NC_000002.10:g.70530852A= NCBI36
NG_029975.1:g.108804T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295400.11:c.*647T= MANE Select ENSP00000295400.6:n.*647T=
ENST00000295400.10:c.*647T= ENSP00000295400.6:n.*647T=
ENST00000418333.6:c.*647T= ENSP00000404099.2:n.*647T=
ENST00000419940.5:c.379-591T=
ENST00000445399.5:c.*19-591T= ENSP00000387493.1:n.*19-591T=
NM_001099691.2:c.*647T= NP_001093161.1:n.*647T=
NM_001308158.1:c.*647T= NP_001295087.1:n.*647T=
NM_001308159.1:c.*647T= NP_001295088.1:n.*647T=
NM_003236.3:c.*647T= NP_003227.1:n.*647T=
NM_003236.4:c.*647T= MANE Select NP_003227.1:n.*647T=
NM_001099691.3:c.*647T= NP_001093161.1:n.*647T=
NM_001308158.2:c.*647T= NP_001295087.1:n.*647T=
NM_001308159.2:c.*647T= NP_001295088.1:n.*647T=