Canonical Allele Identifier: CA2013634717
Gene: NTF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5494466G= , CM000674.2:g.5494466G= GRCh38
NC_000012.11:g.5603632G= , CM000674.1:g.5603632G= GRCh37
NC_000012.10:g.5473893G= NCBI36
NG_050629.1:g.67353G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000423158.4:c.291G= MANE Select ENSP00000397297.2:p.Pro97=
ENST00000331010.7:c.252G= ENSP00000328738.6:p.Pro84=
ENST00000423158.3:c.291G= ENSP00000397297.2:p.Pro97=
ENST00000535299.5:n.232-12099G=
ENST00000543548.1:n.481G=
NM_001102654.1:c.291G= NP_001096124.1:p.Pro97=
NM_002527.4:c.252G= NP_002518.1:p.Pro84=
XM_011520963.1:c.252G= XP_011519265.1:p.Pro84=
XM_011520963.2:c.252G= XP_011519265.1:p.Pro84=
NM_001102654.2:c.291G= MANE Select NP_001096124.1:p.Pro97=
NM_002527.5:c.252G= NP_002518.1:p.Pro84=