Canonical Allele Identifier: CA492076042

Gene: RLBP1

Linked Data

• MyVariant Identifiers: chr15:g.89755019A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89211788A>C , CM000677.2:g.89211788A>C	GRCh38
NC_000015.9:g.89755019A>C , CM000677.1:g.89755019A>C	GRCh37
NC_000015.8:g.87556023A>C	NCBI36
NG_008116.1:g.14904T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000268125.10:c.639T>G MANE Select	ENSP00000268125.5:p.Ala213=
ENST00000268125.9:c.639T>G	ENSP00000268125.5:p.Ala213=
ENST00000563254.1:c.56T>G
ENST00000567787.1:c.*217T>G	ENSP00000457251.1:n.*217T>G
NM_000326.4:c.639T>G	NP_000317.1:p.Ala213=
XM_011521870.1:c.639T>G	XP_011520172.1:p.Ala213=
XM_011521871.1:c.564T>G	XP_011520173.1:p.Ala188=
XM_011521872.1:c.564T>G	XP_011520174.1:p.Ala188=
XM_011521870.2:c.639T>G	XP_011520172.1:p.Ala213=
XM_017022460.1:c.666T>G	XP_016877949.1:p.Ala222=
NM_000326.5:c.639T>G MANE Select	NP_000317.1:p.Ala213=