Canonical Allele Identifier: CA883074690

Gene: NTF4

Linked Data

• dbSNP Id: rs1299304300
• gnomAD v3: 19-49061212-TG-T
• gnomAD v4: 19-49061212-TG-T
• MyVariant Identifiers: chr19:g.49564470del (hg19) ; chr19:g.49061213del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49061214del , CM000681.2:g.49061214del	GRCh38
NC_000019.9:g.49564471del , CM000681.1:g.49564471del	GRCh37
NC_000019.8:g.54256283del	NCBI36
NG_016289.1:g.7655del

Transcript Alleles

HGVS	Amino-acid change
ENST00000593537.2:c.*152del MANE Select	ENSP00000469455.1:n.*152del
ENST00000594938.2:c.*152del	ENSP00000512387.1:n.*152del
ENST00000595857.6:c.*152del	ENSP00000471508.2:n.*152del
ENST00000696088.1:c.*152del	ENSP00000512384.1:n.*152del
ENST00000696089.1:c.*152del	ENSP00000512385.1:n.*152del
ENST00000696090.1:c.*152del	ENSP00000512386.1:n.*152del
ENST00000696091.1:c.*152del	ENSP00000512388.1:n.*152del
ENST00000593537.1:c.785del	ENSP00000469455.1:n.785del
ENST00000599795.5:c.243+542del	ENSP00000470689.1:n.243+542del
NM_006179.4:c.*152del	NP_006170.1:n.*152del
XM_005258962.2:c.*152del	XP_005259019.1:n.*152del
XM_006723232.2:c.*152del	XP_006723295.1:n.*152del
XM_011527008.1:c.*152del	XP_011525310.1:n.*152del
XM_011527009.1:c.*152del	XP_011525311.1:n.*152del
XM_011527010.1:c.*152del	XP_011525312.1:n.*152del
XM_005258962.3:c.*152del	XP_005259019.1:n.*152del
XM_006723232.3:c.*152del	XP_006723295.1:n.*152del
XM_011527008.2:c.*152del	XP_011525310.1:n.*152del
XM_011527009.2:c.*152del	XP_011525311.1:n.*152del
XM_011527010.2:c.*152del	XP_011525312.1:n.*152del
XR_001753693.1:n.830del
XR_001753694.1:n.830del
NM_001395489.1:c.*152del	NP_001382418.1:n.*152del
NM_006179.5:c.*152del MANE Select	NP_006170.1:n.*152del