Canonical Allele Identifier: CA9565587

Gene: NTF4

Linked Data

• dbSNP Id: rs781438973
• ExAC: 19:49564615 A / G
• gnomAD v2: 19-49564615-A-G
• gnomAD v4: 19-49061358-A-G
• MyVariant Identifiers: chr19:g.49564615A>G (hg19) ; chr19:g.49061358A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49061358A>G , CM000681.2:g.49061358A>G	GRCh38
NC_000019.9:g.49564615A>G , CM000681.1:g.49564615A>G	GRCh37
NC_000019.8:g.54256427A>G	NCBI36
NG_016289.1:g.7510T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000593537.2:c.*7T>C MANE Select	ENSP00000469455.1:n.*7T>C
ENST00000594938.2:c.*7T>C	ENSP00000512387.1:n.*7T>C
ENST00000595857.6:c.*7T>C	ENSP00000471508.2:n.*7T>C
ENST00000696088.1:c.*7T>C	ENSP00000512384.1:n.*7T>C
ENST00000696089.1:c.*7T>C	ENSP00000512385.1:n.*7T>C
ENST00000696090.1:c.*7T>C	ENSP00000512386.1:n.*7T>C
ENST00000696091.1:c.*7T>C	ENSP00000512388.1:n.*7T>C
ENST00000593537.1:c.640T>C	ENSP00000469455.1:n.640T>C
ENST00000599795.5:c.243+397T>C	ENSP00000470689.1:n.243+397T>C
NM_006179.4:c.*7T>C	NP_006170.1:n.*7T>C
XM_005258962.2:c.*7T>C	XP_005259019.1:n.*7T>C
XM_006723232.2:c.*7T>C	XP_006723295.1:n.*7T>C
XM_011527008.1:c.*7T>C	XP_011525310.1:n.*7T>C
XM_011527009.1:c.*7T>C	XP_011525311.1:n.*7T>C
XM_011527010.1:c.*7T>C	XP_011525312.1:n.*7T>C
XM_005258962.3:c.*7T>C	XP_005259019.1:n.*7T>C
XM_006723232.3:c.*7T>C	XP_006723295.1:n.*7T>C
XM_011527008.2:c.*7T>C	XP_011525310.1:n.*7T>C
XM_011527009.2:c.*7T>C	XP_011525311.1:n.*7T>C
XM_011527010.2:c.*7T>C	XP_011525312.1:n.*7T>C
XR_001753693.1:n.685T>C
XR_001753694.1:n.685T>C
NM_001395489.1:c.*7T>C	NP_001382418.1:n.*7T>C
NM_006179.5:c.*7T>C MANE Select	NP_006170.1:n.*7T>C