Canonical Allele Identifier: CA2839136378

Gene: USH1C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17498144dup , CM000673.2:g.17498144dup	GRCh38
NC_000011.9:g.17519691dup , CM000673.1:g.17519691dup	GRCh37
NC_000011.8:g.17476267dup	NCBI36
NG_011883.1:g.51275dup
NG_011883.2:g.51275dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2490+20dup MANE Select	ENSP00000005226.7:n.2490+20dup
ENST00000318024.9:c.1590+20dup MANE Plus Clinical	ENSP00000317018.4:n.1590+20dup
ENST00000005226.11:c.2490+20dup	ENSP00000005226.7:n.2490+20dup
ENST00000318024.8:c.1590+20dup	ENSP00000317018.4:n.1590+20dup
ENST00000526313.5:c.*304+20dup	ENSP00000432236.1:n.*304+20dup
ENST00000527020.5:c.1533+20dup	ENSP00000436934.1:n.1533+20dup
ENST00000527720.5:c.1497+20dup	ENSP00000432944.1:n.1497+20dup
ENST00000529563.5:n.474+20dup
NM_001297764.1:c.1533+20dup	NP_001284693.1:n.1533+20dup
NM_005709.3:c.1590+20dup	NP_005700.2:n.1590+20dup
NM_153676.3:c.2490+20dup	NP_710142.1:n.2490+20dup
NR_123738.1:n.1625+20dup
XM_011519831.1:c.2514+20dup	XP_011518133.1:n.2514+20dup
XM_011519832.1:c.1743+20dup	XP_011518134.1:n.1743+20dup
XM_011519832.3:c.1743+20dup	XP_011518134.1:n.1743+20dup
XM_017017075.1:c.2490+20dup	XP_016872564.1:n.2490+20dup
XR_001747717.2:n.1749+20dup
NM_153676.4:c.2490+20dup MANE Select	NP_710142.1:n.2490+20dup
NM_001297764.2:c.1533+20dup	NP_001284693.1:n.1533+20dup
NM_005709.4:c.1590+20dup MANE Plus Clinical	NP_005700.2:n.1590+20dup
NR_123738.2:n.1625+20dup