Canonical Allele Identifier: CA406804769
Gene: NTF4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49061394T>A , CM000681.2:g.49061394T>A GRCh38
NC_000019.9:g.49564651T>A , CM000681.1:g.49564651T>A GRCh37
NC_000019.8:g.54256463T>A NCBI36
NG_016289.1:g.7474A>T

Transcript Alleles

HGVS Amino-acid change
NM_006179.4:c.604A>T NP_006170.1:p.Thr202Ser
XM_005258962.2:c.604A>T XP_005259019.1:p.Thr202Ser
XM_006723232.2:c.604A>T XP_006723295.1:p.Thr202Ser
XM_011527008.1:c.634A>T XP_011525310.1:p.Thr212Ser
XM_011527009.1:c.604A>T XP_011525311.1:p.Thr202Ser
XM_011527010.1:c.604A>T XP_011525312.1:p.Thr202Ser
XM_005258962.3:c.604A>T XP_005259019.1:p.Thr202Ser
XM_006723232.3:c.604A>T XP_006723295.1:p.Thr202Ser
XM_011527008.2:c.634A>T XP_011525310.1:p.Thr212Ser
XM_011527009.2:c.604A>T XP_011525311.1:p.Thr202Ser
XM_011527010.2:c.604A>T XP_011525312.1:p.Thr202Ser
XR_001753693.1:n.649A>T
XR_001753694.1:n.649A>T
ENST00000593537.1:n.604A>T ENSP00000469455.1:p.Thr202Ser
ENST00000599795.5:c.243+361A>T ENSP00000470689.1:p.=