Canonical Allele Identifier: CA1955170000

Gene: USH1C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17494587A= , CM000673.2:g.17494587A=	GRCh38
NC_000011.9:g.17516134A= , CM000673.1:g.17516134A=	GRCh37
NC_000011.8:g.17472710A=	NCBI36
NG_011883.1:g.54830T=
NG_011883.2:g.54830T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2656-211T= MANE Select	ENSP00000005226.7:n.2656-211T=
ENST00000318024.9:c.1647-211T= MANE Plus Clinical	ENSP00000317018.4:n.1647-211T=
ENST00000005226.11:c.2656-211T=	ENSP00000005226.7:n.2656-211T=
ENST00000318024.8:c.1647-211T=	ENSP00000317018.4:n.1647-211T=
ENST00000526313.5:c.*361-211T=	ENSP00000432236.1:n.*361-211T=
ENST00000527020.5:c.1590-211T=	ENSP00000436934.1:n.1590-211T=
ENST00000527551.1:n.157-211T=
ENST00000527720.5:c.1554-211T=	ENSP00000432944.1:n.1554-211T=
ENST00000529563.5:n.531-211T=
ENST00000624811.1:n.507T=
NM_001297764.1:c.1590-211T=	NP_001284693.1:n.1590-211T=
NM_005709.3:c.1647-211T=	NP_005700.2:n.1647-211T=
NM_153676.3:c.2656-211T=	NP_710142.1:n.2656-211T=
NR_123738.1:n.1682-211T=
XM_011519831.1:c.2571-211T=	XP_011518133.1:n.2571-211T=
XM_011519832.1:c.1800-211T=	XP_011518134.1:n.1800-211T=
XM_011519832.3:c.1800-211T=	XP_011518134.1:n.1800-211T=
XM_017017075.1:c.*766T=	XP_016872564.1:n.*766T=
XR_001747717.2:n.1806-211T=
NM_153676.4:c.2656-211T= MANE Select	NP_710142.1:n.2656-211T=
NM_001297764.2:c.1590-211T=	NP_001284693.1:n.1590-211T=
NM_005709.4:c.1647-211T= MANE Plus Clinical	NP_005700.2:n.1647-211T=
NR_123738.2:n.1682-211T=