Canonical Allele Identifier: CA1148437400

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863932_244863945delinsCCTCCTCCTCCTCC , CM000663.2:g.244863932_244863945delinsCCTCCTCCTCCTCC	GRCh38
NC_000001.10:g.245027234_245027247delinsCCTCCTCCTCCTCC , CM000663.1:g.245027234_245027247delinsCCTCCTCCTCCTCC	GRCh37
NC_000001.9:g.243093857_243093870delinsCCTCCTCCTCCTCC	NCBI36
NG_042184.1:g.5581_5594delinsGGAGGAGGAGGAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.41_54delinsGGAGGAGGAGGAGG
ENST00000283179.14:c.363_376delinsGGAGGAGGAGGAGG	ENSP00000283179.10:p.Met121=
ENST00000444376.7:c.363_376delinsGGAGGAGGAGGAGG	ENSP00000393151.2:p.Met121=
ENST00000476241.2:n.548_561delinsGGAGGAGGAGGAGG
ENST00000638475.1:c.147_160delinsGGAGGAGGAGGAGG	ENSP00000491305.1:p.Met49=
ENST00000638952.1:n.594_607delinsGGAGGAGGAGGAGG
ENST00000640218.2:c.363_376delinsGGAGGAGGAGGAGG MANE Select	ENSP00000491215.1:p.Met121=
ENST00000640306.1:c.363_376delinsGGAGGAGGAGGAGG	ENSP00000491685.1:p.Met121=
ENST00000640440.1:c.63_76delinsGGAGGAGGAGGAGG	ENSP00000491263.1:p.Met21=
ENST00000649899.1:n.587_600delinsGGAGGAGGAGGAGG
ENST00000283179.13:c.363_376delinsGGAGGAGGAGGAGG	ENSP00000283179.9:p.Met121=
ENST00000444376.6:c.363_376delinsGGAGGAGGAGGAGG	ENSP00000393151.2:p.Met121=
ENST00000476241.1:n.547_560delinsGGAGGAGGAGGAGG
NM_004501.3:c.363_376delinsGGAGGAGGAGGAGG	NP_004492.2:p.Met121=
NM_031844.2:c.363_376delinsGGAGGAGGAGGAGG	NP_114032.2:p.Met121=
NM_031844.3:c.363_376delinsGGAGGAGGAGGAGG MANE Select	NP_114032.2:p.Met121=