Canonical Allele Identifier: CA49795482

Gene: TGFA

Linked Data

• dbSNP Id: rs782773431
• gnomAD v4: 2-70450236-TC-T
• MyVariant Identifiers: chr2:g.70677369del (hg19) ; chr2:g.70450237del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70450238del , CM000664.2:g.70450238del	GRCh38
NC_000002.11:g.70677370del , CM000664.1:g.70677370del	GRCh37
NC_000002.10:g.70530878del	NCBI36
NG_029975.1:g.108779del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295400.11:c.*622del MANE Select	ENSP00000295400.6:n.*622del
ENST00000295400.10:c.*622del	ENSP00000295400.6:n.*622del
ENST00000418333.6:c.*622del	ENSP00000404099.2:n.*622del
ENST00000419940.5:c.379-616del
ENST00000445399.5:c.*19-616del	ENSP00000387493.1:n.*19-616del
NM_001099691.2:c.*622del	NP_001093161.1:n.*622del
NM_001308158.1:c.*622del	NP_001295087.1:n.*622del
NM_001308159.1:c.*622del	NP_001295088.1:n.*622del
NM_003236.3:c.*622del	NP_003227.1:n.*622del
NM_003236.4:c.*622del MANE Select	NP_003227.1:n.*622del
NM_001099691.3:c.*622del	NP_001093161.1:n.*622del
NM_001308158.2:c.*622del	NP_001295087.1:n.*622del
NM_001308159.2:c.*622del	NP_001295088.1:n.*622del