Canonical Allele Identifier: CA438134959
Gene: LRPAP1 HGNC NCBI

Linked Data

gnomAD v4: 4-3518083-G-A
MyVariant Identifiers: chr4:g.3519810G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3518083G>A , CM000666.2:g.3518083G>A GRCh38
NC_000004.11:g.3519810G>A , CM000666.1:g.3519810G>A GRCh37
NC_000004.10:g.3489608G>A NCBI36
NG_033873.1:g.19415C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000648517.1:c.702C>T ENSP00000496947.1:p.Gly234=
ENST00000650182.1:c.702C>T MANE Select ENSP00000497444.1:p.Gly234=
ENST00000296325.9:n.665C>T
ENST00000500728.2:c.702C>T ENSP00000421922.1:p.Gly234=
ENST00000509198.1:n.748C>T
ENST00000515119.5:c.*479C>T ENSP00000421648.1:n.*479C>T
NM_002337.3:c.702C>T NP_002328.1:p.Gly234=
NR_110005.1:n.665C>T
NM_002337.4:c.702C>T MANE Select NP_002328.1:p.Gly234=
XR_002959730.1:n.787C>T
NR_110005.2:n.665C>T