Canonical Allele Identifier: CA406804774

Gene: NTF4

Linked Data

• MyVariant Identifiers: chr19:g.49564652G>T (hg19) ; chr19:g.49061395G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49061395G>T , CM000681.2:g.49061395G>T	GRCh38
NC_000019.9:g.49564652G>T , CM000681.1:g.49564652G>T	GRCh37
NC_000019.8:g.54256464G>T	NCBI36
NG_016289.1:g.7473C>A

Transcript Alleles

HGVS	Amino-acid change
NM_006179.4:c.603C>A	NP_006170.1:p.Cys201Ter
XM_005258962.2:c.603C>A	XP_005259019.1:p.Cys201Ter
XM_006723232.2:c.603C>A	XP_006723295.1:p.Cys201Ter
XM_011527008.1:c.633C>A	XP_011525310.1:p.Cys211Ter
XM_011527009.1:c.603C>A	XP_011525311.1:p.Cys201Ter
XM_011527010.1:c.603C>A	XP_011525312.1:p.Cys201Ter
XM_005258962.3:c.603C>A	XP_005259019.1:p.Cys201Ter
XM_006723232.3:c.603C>A	XP_006723295.1:p.Cys201Ter
XM_011527008.2:c.633C>A	XP_011525310.1:p.Cys211Ter
XM_011527009.2:c.603C>A	XP_011525311.1:p.Cys201Ter
XM_011527010.2:c.603C>A	XP_011525312.1:p.Cys201Ter
XR_001753693.1:n.648C>A
XR_001753694.1:n.648C>A
ENST00000593537.1:n.603C>A	ENSP00000469455.1:p.Cys201Ter
ENST00000599795.5:c.243+360C>A	ENSP00000470689.1:p.=