Canonical Allele Identifier: CA2013631920
Gene: NTF3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5488155G= , CM000674.2:g.5488155G= GRCh38
NC_000012.11:g.5597321G= , CM000674.1:g.5597321G= GRCh37
NC_000012.10:g.5467582G= NCBI36
NG_050629.1:g.61042G=

Transcript Alleles

HGVS Amino-acid change
ENST00000423158.4:c.19-6039G= MANE Select ENSP00000397297.2:n.19-6039G=
ENST00000423158.3:c.19-6039G= ENSP00000397297.2:n.19-6039G=
ENST00000535299.5:n.232-18410G=
ENST00000543548.1:n.209-6039G=
NM_001102654.1:c.19-6039G= NP_001096124.1:n.19-6039G=
XM_011520963.1:c.-21-6039G= XP_011519265.1:n.-21-6039G=
XM_011520963.2:c.-21-6039G= XP_011519265.1:n.-21-6039G=
NM_001102654.2:c.19-6039G= MANE Select NP_001096124.1:n.19-6039G=
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