Canonical Allele Identifier: CA1259617242

Gene: TGFA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70537556C>G , CM000664.2:g.70537556C>G	GRCh38
NC_000002.11:g.70764688C>G , CM000664.1:g.70764688C>G	GRCh37
NC_000002.10:g.70618196C>G	NCBI36
NG_029975.1:g.21460G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295400.11:c.40+16172G>C MANE Select	ENSP00000295400.6:n.40+16172G>C
ENST00000295400.10:c.40+16172G>C	ENSP00000295400.6:n.40+16172G>C
ENST00000394241.3:c.40+16172G>C	ENSP00000377787.3:n.40+16172G>C
ENST00000418333.6:c.40+16172G>C	ENSP00000404099.2:n.40+16172G>C
ENST00000444975.5:c.58+15628G>C	ENSP00000404131.1:n.58+15628G>C
ENST00000445399.5:c.40+16172G>C	ENSP00000387493.1:n.40+16172G>C
ENST00000450929.5:c.58+15628G>C	ENSP00000414127.1:n.58+15628G>C
ENST00000460808.5:n.99+16172G>C
ENST00000474101.1:n.93+16545G>C
NM_001099691.2:c.40+16172G>C	NP_001093161.1:n.40+16172G>C
NM_001308158.1:c.58+15628G>C	NP_001295087.1:n.58+15628G>C
NM_001308159.1:c.58+15628G>C	NP_001295088.1:n.58+15628G>C
NM_003236.3:c.40+16172G>C	NP_003227.1:n.40+16172G>C
NM_003236.4:c.40+16172G>C MANE Select	NP_003227.1:n.40+16172G>C
NM_001099691.3:c.40+16172G>C	NP_001093161.1:n.40+16172G>C
NM_001308158.2:c.58+15628G>C	NP_001295087.1:n.58+15628G>C
NM_001308159.2:c.58+15628G>C	NP_001295088.1:n.58+15628G>C