Canonical Allele Identifier: CA49826601

Gene: TGFA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70505720A>G , CM000664.2:g.70505720A>G	GRCh38
NC_000002.11:g.70732852A>G , CM000664.1:g.70732852A>G	GRCh37
NC_000002.10:g.70586360A>G	NCBI36
NG_029975.1:g.53296T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295400.11:c.94+9139T>C MANE Select	ENSP00000295400.6:n.94+9139T>C
ENST00000295400.10:c.94+9139T>C	ENSP00000295400.6:n.94+9139T>C
ENST00000394241.3:c.94+9139T>C	ENSP00000377787.3:n.94+9139T>C
ENST00000418333.6:c.94+9139T>C	ENSP00000404099.2:n.94+9139T>C
ENST00000444975.5:c.112+9139T>C	ENSP00000404131.1:n.112+9139T>C
ENST00000445399.5:c.94+9139T>C	ENSP00000387493.1:n.94+9139T>C
ENST00000450929.5:c.112+9139T>C	ENSP00000414127.1:n.112+9139T>C
ENST00000460808.5:n.153+9139T>C
NM_001099691.2:c.94+9139T>C	NP_001093161.1:n.94+9139T>C
NM_001308158.1:c.112+9139T>C	NP_001295087.1:n.112+9139T>C
NM_001308159.1:c.112+9139T>C	NP_001295088.1:n.112+9139T>C
NM_003236.3:c.94+9139T>C	NP_003227.1:n.94+9139T>C
NM_003236.4:c.94+9139T>C MANE Select	NP_003227.1:n.94+9139T>C
NM_001099691.3:c.94+9139T>C	NP_001093161.1:n.94+9139T>C
NM_001308158.2:c.112+9139T>C	NP_001295087.1:n.112+9139T>C
NM_001308159.2:c.112+9139T>C	NP_001295088.1:n.112+9139T>C