Canonical Allele Identifier: CA15175937
Gene: TGFA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.70509087A>G , CM000664.2:g.70509087A>G GRCh38
NC_000002.11:g.70736219A>G , CM000664.1:g.70736219A>G GRCh37
NC_000002.10:g.70589727A>G NCBI36
NG_029975.1:g.49929T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000295400.11:c.94+5772T>C MANE Select ENSP00000295400.6:n.94+5772T>C
ENST00000295400.10:c.94+5772T>C ENSP00000295400.6:n.94+5772T>C
ENST00000394241.3:c.94+5772T>C ENSP00000377787.3:n.94+5772T>C
ENST00000418333.6:c.94+5772T>C ENSP00000404099.2:n.94+5772T>C
ENST00000444975.5:c.112+5772T>C ENSP00000404131.1:n.112+5772T>C
ENST00000445399.5:c.94+5772T>C ENSP00000387493.1:n.94+5772T>C
ENST00000450929.5:c.112+5772T>C ENSP00000414127.1:n.112+5772T>C
ENST00000460808.5:n.153+5772T>C
NM_001099691.2:c.94+5772T>C NP_001093161.1:n.94+5772T>C
NM_001308158.1:c.112+5772T>C NP_001295087.1:n.112+5772T>C
NM_001308159.1:c.112+5772T>C NP_001295088.1:n.112+5772T>C
NM_003236.3:c.94+5772T>C NP_003227.1:n.94+5772T>C
NM_003236.4:c.94+5772T>C MANE Select NP_003227.1:n.94+5772T>C
NM_001099691.3:c.94+5772T>C NP_001093161.1:n.94+5772T>C
NM_001308158.2:c.112+5772T>C NP_001295087.1:n.112+5772T>C
NM_001308159.2:c.112+5772T>C NP_001295088.1:n.112+5772T>C
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