Canonical Allele Identifier: CA344912592

Gene: USH2A

Linked Data

• MyVariant Identifiers: chr1:g.216498849A>G (hg19) ; chr1:g.216325507A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.216325507A>G , CM000663.2:g.216325507A>G	GRCh38
NC_000001.10:g.216498849A>G , CM000663.1:g.216498849A>G	GRCh37
NC_000001.9:g.214565472A>G	NCBI36
NG_009497.1:g.102890T>C
NG_009497.2:g.102942T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307340.8:c.941T>C MANE Select	ENSP00000305941.3:p.Leu314Ser
ENST00000674083.1:c.941T>C	ENSP00000501296.1:p.Leu314Ser
ENST00000307340.7:c.941T>C	ENSP00000305941.3:p.Leu314Ser
ENST00000366942.3:c.941T>C	ENSP00000355909.3:p.Leu314Ser
NM_007123.5:c.941T>C	NP_009054.5:p.Leu314Ser
NM_206933.2:c.941T>C	NP_996816.2:p.Leu314Ser
NM_206933.3:c.941T>C	NP_996816.2:p.Leu314Ser
NM_007123.6:c.941T>C	NP_009054.6:p.Leu314Ser
NM_206933.4:c.941T>C MANE Select	NP_996816.3:p.Leu314Ser