Canonical Allele Identifier: CA1259573940
Gene: TGFA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70450221A= , CM000664.2:g.70450221A= GRCh38
NC_000002.11:g.70677353A= , CM000664.1:g.70677353A= GRCh37
NC_000002.10:g.70530861A= NCBI36
NG_029975.1:g.108795T=

Transcript Alleles

HGVS Amino-acid change
ENST00000295400.11:c.*638T= MANE Select ENSP00000295400.6:n.*638T=
ENST00000295400.10:c.*638T= ENSP00000295400.6:n.*638T=
ENST00000418333.6:c.*638T= ENSP00000404099.2:n.*638T=
ENST00000419940.5:c.379-600T=
ENST00000445399.5:c.*19-600T= ENSP00000387493.1:n.*19-600T=
NM_001099691.2:c.*638T= NP_001093161.1:n.*638T=
NM_001308158.1:c.*638T= NP_001295087.1:n.*638T=
NM_001308159.1:c.*638T= NP_001295088.1:n.*638T=
NM_003236.3:c.*638T= NP_003227.1:n.*638T=
NM_003236.4:c.*638T= MANE Select NP_003227.1:n.*638T=
NM_001099691.3:c.*638T= NP_001093161.1:n.*638T=
NM_001308158.2:c.*638T= NP_001295087.1:n.*638T=
NM_001308159.2:c.*638T= NP_001295088.1:n.*638T=