Canonical Allele Identifier: CA533290846

Gene: TGFA

Linked Data

• dbSNP Id: rs1553489374
• gnomAD v2: 2-70677356-A-T
• MyVariant Identifiers: chr2:g.70677356A>T (hg19) ; chr2:g.70450224A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70450224A>T , CM000664.2:g.70450224A>T	GRCh38
NC_000002.11:g.70677356A>T , CM000664.1:g.70677356A>T	GRCh37
NC_000002.10:g.70530864A>T	NCBI36
NG_029975.1:g.108792T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000295400.11:c.*635T>A MANE Select	ENSP00000295400.6:n.*635T>A
ENST00000295400.10:c.*635T>A	ENSP00000295400.6:n.*635T>A
ENST00000418333.6:c.*635T>A	ENSP00000404099.2:n.*635T>A
ENST00000419940.5:c.379-603T>A
ENST00000445399.5:c.*19-603T>A	ENSP00000387493.1:n.*19-603T>A
NM_001099691.2:c.*635T>A	NP_001093161.1:n.*635T>A
NM_001308158.1:c.*635T>A	NP_001295087.1:n.*635T>A
NM_001308159.1:c.*635T>A	NP_001295088.1:n.*635T>A
NM_003236.3:c.*635T>A	NP_003227.1:n.*635T>A
NM_003236.4:c.*635T>A MANE Select	NP_003227.1:n.*635T>A
NM_001099691.3:c.*635T>A	NP_001093161.1:n.*635T>A
NM_001308158.2:c.*635T>A	NP_001295087.1:n.*635T>A
NM_001308159.2:c.*635T>A	NP_001295088.1:n.*635T>A