Canonical Allele Identifier: CA422275826

Gene: RNASEL

Linked Data

• MyVariant Identifiers: chr1:g.182555087C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.182585952C>T , CM000663.2:g.182585952C>T	GRCh38
NC_000001.10:g.182555087C>T , CM000663.1:g.182555087C>T	GRCh37
NC_000001.9:g.180821710C>T	NCBI36
NG_009024.2:g.6022G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367559.7:c.855G>A MANE Select	ENSP00000356530.3:p.Leu285=
ENST00000539397.1:c.855G>A	ENSP00000440844.1:p.Leu285=
NM_021133.3:c.855G>A	NP_066956.1:p.Leu285=
XM_005245411.2:c.855G>A	XP_005245468.1:p.Leu285=
XR_001737359.1:n.1138G>A
XR_001737360.1:n.1138G>A
NM_021133.4:c.855G>A MANE Select	NP_066956.1:p.Leu285=