Canonical Allele Identifier: CA406804731

Gene: NTF4

Linked Data

• MyVariant Identifiers: chr19:g.49564641C>A (hg19) ; chr19:g.49061384C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49061384C>A , CM000681.2:g.49061384C>A	GRCh38
NC_000019.9:g.49564641C>A , CM000681.1:g.49564641C>A	GRCh37
NC_000019.8:g.54256453C>A	NCBI36
NG_016289.1:g.7484G>T

Transcript Alleles

HGVS	Amino-acid change
NM_006179.4:c.614G>T	NP_006170.1:p.Ser205Ile
XM_005258962.2:c.614G>T	XP_005259019.1:p.Ser205Ile
XM_006723232.2:c.614G>T	XP_006723295.1:p.Ser205Ile
XM_011527008.1:c.644G>T	XP_011525310.1:p.Ser215Ile
XM_011527009.1:c.614G>T	XP_011525311.1:p.Ser205Ile
XM_011527010.1:c.614G>T	XP_011525312.1:p.Ser205Ile
XM_005258962.3:c.614G>T	XP_005259019.1:p.Ser205Ile
XM_006723232.3:c.614G>T	XP_006723295.1:p.Ser205Ile
XM_011527008.2:c.644G>T	XP_011525310.1:p.Ser215Ile
XM_011527009.2:c.614G>T	XP_011525311.1:p.Ser205Ile
XM_011527010.2:c.614G>T	XP_011525312.1:p.Ser205Ile
XR_001753693.1:n.659G>T
XR_001753694.1:n.659G>T
ENST00000593537.1:n.614G>T	ENSP00000469455.1:p.Ser205Ile
ENST00000599795.5:c.243+371G>T	ENSP00000470689.1:p.=