Canonical Allele Identifier: CA406806510

Gene: NTF4

Linked Data

• MyVariant Identifiers: chr19:g.49564923A>G (hg19) ; chr19:g.49061666A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49061666A>G , CM000681.2:g.49061666A>G	GRCh38
NC_000019.9:g.49564923A>G , CM000681.1:g.49564923A>G	GRCh37
NC_000019.8:g.54256735A>G	NCBI36
NG_016289.1:g.7202T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593537.2:c.332T>C MANE Select	ENSP00000469455.1:p.Val111Ala
ENST00000594938.2:c.332T>C	ENSP00000512387.1:p.Val111Ala
ENST00000595857.6:c.332T>C	ENSP00000471508.2:p.Val111Ala
ENST00000696088.1:c.332T>C	ENSP00000512384.1:p.Val111Ala
ENST00000696089.1:c.332T>C	ENSP00000512385.1:p.Val111Ala
ENST00000696090.1:c.332T>C	ENSP00000512386.1:p.Val111Ala
ENST00000696091.1:c.332T>C	ENSP00000512388.1:p.Val111Ala
ENST00000593537.1:c.332T>C	ENSP00000469455.1:p.Val111Ala
ENST00000595857.5:c.332T>C	ENSP00000471508.1:p.Val111Ala
ENST00000599795.5:c.243+89T>C	ENSP00000470689.1:n.243+89T>C
NM_006179.4:c.332T>C	NP_006170.1:p.Val111Ala
XM_005258962.2:c.332T>C	XP_005259019.1:p.Val111Ala
XM_006723232.2:c.332T>C	XP_006723295.1:p.Val111Ala
XM_011527008.1:c.362T>C	XP_011525310.1:p.Val121Ala
XM_011527009.1:c.332T>C	XP_011525311.1:p.Val111Ala
XM_011527010.1:c.332T>C	XP_011525312.1:p.Val111Ala
XM_005258962.3:c.332T>C	XP_005259019.1:p.Val111Ala
XM_006723232.3:c.332T>C	XP_006723295.1:p.Val111Ala
XM_011527008.2:c.362T>C	XP_011525310.1:p.Val121Ala
XM_011527009.2:c.332T>C	XP_011525311.1:p.Val111Ala
XM_011527010.2:c.332T>C	XP_011525312.1:p.Val111Ala
XR_001753693.1:n.377T>C
XR_001753694.1:n.377T>C
NM_001395489.1:c.332T>C	NP_001382418.1:p.Val111Ala
NM_006179.5:c.332T>C MANE Select	NP_006170.1:p.Val111Ala