Canonical Allele Identifier: CA422276143

Gene: RNASEL

Linked Data

• MyVariant Identifiers: chr1:g.182555414A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.182586279A>T , CM000663.2:g.182586279A>T	GRCh38
NC_000001.10:g.182555414A>T , CM000663.1:g.182555414A>T	GRCh37
NC_000001.9:g.180822037A>T	NCBI36
NG_009024.2:g.5695T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367559.7:c.528T>A MANE Select	ENSP00000356530.3:p.Ala176=
ENST00000539397.1:c.528T>A	ENSP00000440844.1:p.Ala176=
NM_021133.3:c.528T>A	NP_066956.1:p.Ala176=
XM_005245411.2:c.528T>A	XP_005245468.1:p.Ala176=
XR_001737359.1:n.811T>A
XR_001737360.1:n.811T>A
NM_021133.4:c.528T>A MANE Select	NP_066956.1:p.Ala176=