Canonical Allele Identifier: CA422275793

Gene: RNASEL

Linked Data

• MyVariant Identifiers: chr1:g.182555066C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.182585931C>G , CM000663.2:g.182585931C>G	GRCh38
NC_000001.10:g.182555066C>G , CM000663.1:g.182555066C>G	GRCh37
NC_000001.9:g.180821689C>G	NCBI36
NG_009024.2:g.6043G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367559.7:c.876G>C MANE Select	ENSP00000356530.3:p.Leu292=
ENST00000539397.1:c.876G>C	ENSP00000440844.1:p.Leu292=
NM_021133.3:c.876G>C	NP_066956.1:p.Leu292=
XM_005245411.2:c.876G>C	XP_005245468.1:p.Leu292=
XR_001737359.1:n.1159G>C
XR_001737360.1:n.1159G>C
NM_021133.4:c.876G>C MANE Select	NP_066956.1:p.Leu292=