Canonical Allele Identifier: CA492075545

Gene: RLBP1

Linked Data

• MyVariant Identifiers: chr15:g.89754029T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89210798T>C , CM000677.2:g.89210798T>C	GRCh38
NC_000015.9:g.89754029T>C , CM000677.1:g.89754029T>C	GRCh37
NC_000015.8:g.87555033T>C	NCBI36
NG_008116.1:g.15894A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000268125.10:c.696A>G MANE Select	ENSP00000268125.5:p.Pro232=
ENST00000268125.9:c.696A>G	ENSP00000268125.5:p.Pro232=
ENST00000563254.1:c.102-34A>G
ENST00000567787.1:c.*274A>G	ENSP00000457251.1:n.*274A>G
NM_000326.4:c.696A>G	NP_000317.1:p.Pro232=
XM_011521870.1:c.696A>G	XP_011520172.1:p.Pro232=
XM_011521871.1:c.621A>G	XP_011520173.1:p.Pro207=
XM_011521872.1:c.621A>G	XP_011520174.1:p.Pro207=
XM_011521870.2:c.696A>G	XP_011520172.1:p.Pro232=
XM_017022460.1:c.723A>G	XP_016877949.1:p.Pro241=
NM_000326.5:c.696A>G MANE Select	NP_000317.1:p.Pro232=