Canonical Allele Identifier: CA379803087

Gene: USH1C

Linked Data

• gnomAD v4: 11-17501108-G-C
• MyVariant Identifiers: chr11:g.17522655G>C (hg19) ; chr11:g.17501108G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17501108G>C , CM000673.2:g.17501108G>C	GRCh38
NC_000011.9:g.17522655G>C , CM000673.1:g.17522655G>C	GRCh37
NC_000011.8:g.17479231G>C	NCBI36
NG_011883.1:g.48309C>G
NG_011883.2:g.48309C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2323C>G MANE Select	ENSP00000005226.7:p.Pro775Ala
ENST00000318024.9:c.1423C>G MANE Plus Clinical	ENSP00000317018.4:p.Pro475Ala
ENST00000005226.11:c.2323C>G	ENSP00000005226.7:p.Pro775Ala
ENST00000318024.8:c.1423C>G	ENSP00000317018.4:p.Pro475Ala
ENST00000526313.5:c.*137C>G	ENSP00000432236.1:n.*137C>G
ENST00000527020.5:c.1366C>G	ENSP00000436934.1:p.Pro456Ala
ENST00000527720.5:c.1330C>G	ENSP00000432944.1:p.Pro444Ala
ENST00000529563.5:n.307C>G
ENST00000534556.1:n.208C>G
NM_001297764.1:c.1366C>G	NP_001284693.1:p.Pro456Ala
NM_005709.3:c.1423C>G	NP_005700.2:p.Pro475Ala
NM_153676.3:c.2323C>G	NP_710142.1:p.Pro775Ala
NR_123738.1:n.1458C>G
XM_011519831.1:c.2347C>G	XP_011518133.1:p.Pro783Ala
XM_011519832.1:c.1576C>G	XP_011518134.1:p.Pro526Ala
XM_011519833.1:c.*30C>G	XP_011518135.1:n.*30C>G
XR_930841.1:n.1794C>G
XR_930842.1:n.1735C>G
XM_011519832.3:c.1576C>G	XP_011518134.1:p.Pro526Ala
XM_017017075.1:c.2323C>G	XP_016872564.1:p.Pro775Ala
XR_001747717.2:n.1582C>G
NM_153676.4:c.2323C>G MANE Select	NP_710142.1:p.Pro775Ala
NM_001297764.2:c.1366C>G	NP_001284693.1:p.Pro456Ala
NM_005709.4:c.1423C>G MANE Plus Clinical	NP_005700.2:p.Pro475Ala
NR_123738.2:n.1458C>G