Canonical Allele Identifier: CA2669747473
Gene: LRPAP1 HGNC NCBI

Linked Data

gnomAD v4: 4-3518013-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3518013C>A , CM000666.2:g.3518013C>A GRCh38
NC_000004.11:g.3519740C>A , CM000666.1:g.3519740C>A GRCh37
NC_000004.10:g.3489538C>A NCBI36
NG_033873.1:g.19485G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648517.1:c.751+21G>T ENSP00000496947.1:n.751+21G>T
ENST00000650182.1:c.751+21G>T MANE Select ENSP00000497444.1:n.751+21G>T
ENST00000296325.9:n.714+21G>T
ENST00000500728.2:c.751+21G>T ENSP00000421922.1:n.751+21G>T
ENST00000509198.1:n.818G>T
ENST00000515119.5:c.*528+21G>T ENSP00000421648.1:n.*528+21G>T
NM_002337.3:c.751+21G>T NP_002328.1:n.751+21G>T
NR_110005.1:n.714+21G>T
NM_002337.4:c.751+21G>T MANE Select NP_002328.1:n.751+21G>T
XR_002959730.1:n.857G>T
NR_110005.2:n.714+21G>T