Canonical Allele Identifier: CA11188976

Gene: TGFA TGFA-IT1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.70470535G>A , CM000664.2:g.70470535G>A	GRCh38
NC_000002.11:g.70697667G>A , CM000664.1:g.70697667G>A	GRCh37
NC_000002.10:g.70551175G>A	NCBI36
NG_029975.1:g.88481C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003236.4:c.95-4799C>T (TGFA) MANE Select	NP_003227.1:n.95-4799C>T
ENST00000295400.11:c.95-4799C>T (TGFA) MANE Select	ENSP00000295400.6:n.95-4799C>T
NM_001099691.2:c.95-4802C>T (TGFA)	NP_001093161.1:n.95-4802C>T
NM_001099691.3:c.95-4802C>T (TGFA)	NP_001093161.1:n.95-4802C>T
NM_001308158.1:c.113-4799C>T (TGFA)	NP_001295087.1:n.113-4799C>T
NM_001308158.2:c.113-4799C>T (TGFA)	NP_001295087.1:n.113-4799C>T
NM_001308159.1:c.113-4802C>T (TGFA)	NP_001295088.1:n.113-4802C>T
NM_001308159.2:c.113-4802C>T (TGFA)	NP_001295088.1:n.113-4802C>T
NM_003236.3:c.95-4799C>T (TGFA)	NP_003227.1:n.95-4799C>T
NR_046798.1:n.57-2040C>T (TGFA-IT1)
ENST00000295400.10:c.95-4799C>T (TGFA)	ENSP00000295400.6:n.95-4799C>T
ENST00000394241.3:c.95-4802C>T (TGFA)	ENSP00000377787.3:n.95-4802C>T
ENST00000418333.6:c.95-4802C>T (TGFA)	ENSP00000404099.2:n.95-4802C>T
ENST00000444975.5:c.113-4799C>T (TGFA)	ENSP00000404131.1:n.113-4799C>T
ENST00000445399.5:c.95-4802C>T (TGFA)	ENSP00000387493.1:n.95-4802C>T
ENST00000450929.5:c.113-4802C>T (TGFA)	ENSP00000414127.1:n.113-4802C>T
ENST00000460808.5:n.154-4799C>T (TGFA)