Canonical Allele Identifier: CA379803041

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17522642A>G (hg19) ; chr11:g.17501095A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17501095A>G , CM000673.2:g.17501095A>G	GRCh38
NC_000011.9:g.17522642A>G , CM000673.1:g.17522642A>G	GRCh37
NC_000011.8:g.17479218A>G	NCBI36
NG_011883.1:g.48322T>C
NG_011883.2:g.48322T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2336T>C MANE Select	ENSP00000005226.7:p.Val779Ala
ENST00000318024.9:c.1436T>C MANE Plus Clinical	ENSP00000317018.4:p.Val479Ala
ENST00000005226.11:c.2336T>C	ENSP00000005226.7:p.Val779Ala
ENST00000318024.8:c.1436T>C	ENSP00000317018.4:p.Val479Ala
ENST00000526313.5:c.*150T>C	ENSP00000432236.1:n.*150T>C
ENST00000527020.5:c.1379T>C	ENSP00000436934.1:p.Val460Ala
ENST00000527720.5:c.1343T>C	ENSP00000432944.1:p.Val448Ala
ENST00000529563.5:n.320T>C
ENST00000534556.1:n.221T>C
NM_001297764.1:c.1379T>C	NP_001284693.1:p.Val460Ala
NM_005709.3:c.1436T>C	NP_005700.2:p.Val479Ala
NM_153676.3:c.2336T>C	NP_710142.1:p.Val779Ala
NR_123738.1:n.1471T>C
XM_011519831.1:c.2360T>C	XP_011518133.1:p.Val787Ala
XM_011519832.1:c.1589T>C	XP_011518134.1:p.Val530Ala
XM_011519833.1:c.*43T>C	XP_011518135.1:n.*43T>C
XR_930841.1:n.1807T>C
XR_930842.1:n.1748T>C
XM_011519832.3:c.1589T>C	XP_011518134.1:p.Val530Ala
XM_017017075.1:c.2336T>C	XP_016872564.1:p.Val779Ala
XR_001747717.2:n.1595T>C
NM_153676.4:c.2336T>C MANE Select	NP_710142.1:p.Val779Ala
NM_001297764.2:c.1379T>C	NP_001284693.1:p.Val460Ala
NM_005709.4:c.1436T>C MANE Plus Clinical	NP_005700.2:p.Val479Ala
NR_123738.2:n.1471T>C