Canonical Allele Identifier: CA422276273

Gene: RNASEL

Linked Data

• MyVariant Identifiers: chr1:g.182555450C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.182586315C>G , CM000663.2:g.182586315C>G	GRCh38
NC_000001.10:g.182555450C>G , CM000663.1:g.182555450C>G	GRCh37
NC_000001.9:g.180822073C>G	NCBI36
NG_009024.2:g.5659G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367559.7:c.492G>C MANE Select	ENSP00000356530.3:p.Leu164=
ENST00000539397.1:c.492G>C	ENSP00000440844.1:p.Leu164=
NM_021133.3:c.492G>C	NP_066956.1:p.Leu164=
XM_005245411.2:c.492G>C	XP_005245468.1:p.Leu164=
XR_001737359.1:n.775G>C
XR_001737360.1:n.775G>C
NM_021133.4:c.492G>C MANE Select	NP_066956.1:p.Leu164=