Canonical Allele Identifier: CA2499214647

Gene: HNRNPU

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244855609del , CM000663.2:g.244855609del	GRCh38
NC_000001.10:g.245018911del , CM000663.1:g.245018911del	GRCh37
NC_000001.9:g.243085534del	NCBI36
NG_042184.1:g.13917del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000639628.2:c.1340-1del	ENSP00000491340.1:n.1340-1del
ENST00000704074.1:c.1789-1del
ENST00000283179.14:c.1925-1del	ENSP00000283179.10:n.1925-1del
ENST00000366525.8:n.1781-1del
ENST00000440865.2:c.1499-1del	ENSP00000410728.2:n.1499-1del
ENST00000444376.7:c.2111-1del	ENSP00000393151.2:n.2111-1del
ENST00000468690.2:n.3854del
ENST00000475997.6:c.155-1del	ENSP00000482621.2:n.155-1del
ENST00000476241.2:n.4282-1del
ENST00000638230.1:c.1278-1del
ENST00000638301.1:c.*453del	ENSP00000491807.1:n.*453del
ENST00000638475.1:c.1877-1del	ENSP00000491305.1:n.1877-1del
ENST00000638716.1:c.1334-1del	ENSP00000491601.1:n.1334-1del
ENST00000638952.1:n.4385-1del
ENST00000639064.1:n.1223-1del
ENST00000639628.1:c.1340-1del	ENSP00000491340.1:n.1340-1del
ENST00000639824.1:c.744-1del
ENST00000639880.1:c.*1104-1del	ENSP00000490988.1:n.*1104-1del
ENST00000640001.1:c.1340-1del	ENSP00000491294.1:n.1340-1del
ENST00000640056.1:c.1491-1del	ENSP00000492620.1:n.1491-1del
ENST00000640119.1:c.379-1del	ENSP00000491491.1:n.379-1del
ENST00000640218.2:c.2168-1del MANE Select	ENSP00000491215.1:n.2168-1del
ENST00000640306.1:c.2111-1del	ENSP00000491685.1:n.2111-1del
ENST00000649899.1:n.2335-1del
ENST00000283179.13:c.2168-1del	ENSP00000283179.9:n.2168-1del
ENST00000366525.7:n.1908-1del
ENST00000444376.6:c.2111-1del	ENSP00000393151.2:n.2111-1del
NM_004501.3:c.2111-1del	NP_004492.2:n.2111-1del
NM_031844.2:c.2168-1del	NP_114032.2:n.2168-1del
NM_031844.3:c.2168-1del MANE Select	NP_114032.2:n.2168-1del