Canonical Allele Identifier: CA916562214

Gene: TGFA

Linked Data

• dbSNP Id: rs1553489377
• gnomAD v4: 2-70450257-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70450258dup , CM000664.2:g.70450258dup	GRCh38
NC_000002.11:g.70677390dup , CM000664.1:g.70677390dup	GRCh37
NC_000002.10:g.70530898dup	NCBI36
NG_029975.1:g.108758dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000295400.11:c.*601dup MANE Select	ENSP00000295400.6:n.*601dup
ENST00000295400.10:c.*601dup	ENSP00000295400.6:n.*601dup
ENST00000418333.6:c.*601dup	ENSP00000404099.2:n.*601dup
ENST00000419940.5:c.379-637dup
ENST00000445399.5:c.*19-637dup	ENSP00000387493.1:n.*19-637dup
NM_001099691.2:c.*601dup	NP_001093161.1:n.*601dup
NM_001308158.1:c.*601dup	NP_001295087.1:n.*601dup
NM_001308159.1:c.*601dup	NP_001295088.1:n.*601dup
NM_003236.3:c.*601dup	NP_003227.1:n.*601dup
NM_003236.4:c.*601dup MANE Select	NP_003227.1:n.*601dup
NM_001099691.3:c.*601dup	NP_001093161.1:n.*601dup
NM_001308158.2:c.*601dup	NP_001295087.1:n.*601dup
NM_001308159.2:c.*601dup	NP_001295088.1:n.*601dup