Canonical Allele Identifier: CA2630242479

Gene: RLBP1

Linked Data

• gnomAD v4: 15-89211643-TCCAACTTCTCAGTTCCCTGCAAGCACCATGAAAGGAGGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.89211647_89211685del , CM000677.2:g.89211647_89211685del	GRCh38
NC_000015.9:g.89754878_89754916del , CM000677.1:g.89754878_89754916del	GRCh37
NC_000015.8:g.87555882_87555920del	NCBI36
NG_008116.1:g.15010_15048del

Transcript Alleles

HGVS	Amino-acid change
ENST00000268125.10:c.684+61_684+99del MANE Select	ENSP00000268125.5:n.684+61_684+99del
ENST00000268125.9:c.684+61_684+99del	ENSP00000268125.5:n.684+61_684+99del
ENST00000563254.1:c.101+61_101+99del
ENST00000567787.1:c.*262+61_*262+99del	ENSP00000457251.1:n.*262+61_*262+99del
NM_000326.4:c.684+61_684+99del	NP_000317.1:n.684+61_684+99del
XM_011521870.1:c.684+61_684+99del	XP_011520172.1:n.684+61_684+99del
XM_011521871.1:c.609+61_609+99del	XP_011520173.1:n.609+61_609+99del
XM_011521872.1:c.609+61_609+99del	XP_011520174.1:n.609+61_609+99del
XM_011521870.2:c.684+61_684+99del	XP_011520172.1:n.684+61_684+99del
XM_017022460.1:c.711+61_711+99del	XP_016877949.1:n.711+61_711+99del
NM_000326.5:c.684+61_684+99del MANE Select	NP_000317.1:n.684+61_684+99del