Canonical Allele Identifier: CA379803046

Gene: USH1C

Linked Data

• MyVariant Identifiers: chr11:g.17522643C>G (hg19) ; chr11:g.17501096C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17501096C>G , CM000673.2:g.17501096C>G	GRCh38
NC_000011.9:g.17522643C>G , CM000673.1:g.17522643C>G	GRCh37
NC_000011.8:g.17479219C>G	NCBI36
NG_011883.1:g.48321G>C
NG_011883.2:g.48321G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000005226.12:c.2335G>C MANE Select	ENSP00000005226.7:p.Val779Leu
ENST00000318024.9:c.1435G>C MANE Plus Clinical	ENSP00000317018.4:p.Val479Leu
ENST00000005226.11:c.2335G>C	ENSP00000005226.7:p.Val779Leu
ENST00000318024.8:c.1435G>C	ENSP00000317018.4:p.Val479Leu
ENST00000526313.5:c.*149G>C	ENSP00000432236.1:n.*149G>C
ENST00000527020.5:c.1378G>C	ENSP00000436934.1:p.Val460Leu
ENST00000527720.5:c.1342G>C	ENSP00000432944.1:p.Val448Leu
ENST00000529563.5:n.319G>C
ENST00000534556.1:n.220G>C
NM_001297764.1:c.1378G>C	NP_001284693.1:p.Val460Leu
NM_005709.3:c.1435G>C	NP_005700.2:p.Val479Leu
NM_153676.3:c.2335G>C	NP_710142.1:p.Val779Leu
NR_123738.1:n.1470G>C
XM_011519831.1:c.2359G>C	XP_011518133.1:p.Val787Leu
XM_011519832.1:c.1588G>C	XP_011518134.1:p.Val530Leu
XM_011519833.1:c.*42G>C	XP_011518135.1:n.*42G>C
XR_930841.1:n.1806G>C
XR_930842.1:n.1747G>C
XM_011519832.3:c.1588G>C	XP_011518134.1:p.Val530Leu
XM_017017075.1:c.2335G>C	XP_016872564.1:p.Val779Leu
XR_001747717.2:n.1594G>C
NM_153676.4:c.2335G>C MANE Select	NP_710142.1:p.Val779Leu
NM_001297764.2:c.1378G>C	NP_001284693.1:p.Val460Leu
NM_005709.4:c.1435G>C MANE Plus Clinical	NP_005700.2:p.Val479Leu
NR_123738.2:n.1470G>C