Canonical Allele Identifier: CA406804756

Gene: NTF4

Linked Data

• MyVariant Identifiers: chr19:g.49564648G>C (hg19) ; chr19:g.49061391G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49061391G>C , CM000681.2:g.49061391G>C	GRCh38
NC_000019.9:g.49564648G>C , CM000681.1:g.49564648G>C	GRCh37
NC_000019.8:g.54256460G>C	NCBI36
NG_016289.1:g.7477C>G

Transcript Alleles

HGVS	Amino-acid change
NM_006179.4:c.607C>G	NP_006170.1:p.Leu203Val
XM_005258962.2:c.607C>G	XP_005259019.1:p.Leu203Val
XM_006723232.2:c.607C>G	XP_006723295.1:p.Leu203Val
XM_011527008.1:c.637C>G	XP_011525310.1:p.Leu213Val
XM_011527009.1:c.607C>G	XP_011525311.1:p.Leu203Val
XM_011527010.1:c.607C>G	XP_011525312.1:p.Leu203Val
XM_005258962.3:c.607C>G	XP_005259019.1:p.Leu203Val
XM_006723232.3:c.607C>G	XP_006723295.1:p.Leu203Val
XM_011527008.2:c.637C>G	XP_011525310.1:p.Leu213Val
XM_011527009.2:c.607C>G	XP_011525311.1:p.Leu203Val
XM_011527010.2:c.607C>G	XP_011525312.1:p.Leu203Val
XR_001753693.1:n.652C>G
XR_001753694.1:n.652C>G
ENST00000593537.1:n.607C>G	ENSP00000469455.1:p.Leu203Val
ENST00000599795.5:c.243+364C>G	ENSP00000470689.1:p.=