Canonical Allele Identifier: CA438134963

Gene: LRPAP1

Linked Data

• MyVariant Identifiers: chr4:g.3519813C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.3518086C>T , CM000666.2:g.3518086C>T	GRCh38
NC_000004.11:g.3519813C>T , CM000666.1:g.3519813C>T	GRCh37
NC_000004.10:g.3489611C>T	NCBI36
NG_033873.1:g.19412G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648517.1:c.699G>A	ENSP00000496947.1:p.Gln233=
ENST00000650182.1:c.699G>A MANE Select	ENSP00000497444.1:p.Gln233=
ENST00000296325.9:n.662G>A
ENST00000500728.2:c.699G>A	ENSP00000421922.1:p.Gln233=
ENST00000509198.1:n.745G>A
ENST00000515119.5:c.*476G>A	ENSP00000421648.1:n.*476G>A
NM_002337.3:c.699G>A	NP_002328.1:p.Gln233=
NR_110005.1:n.662G>A
NM_002337.4:c.699G>A MANE Select	NP_002328.1:p.Gln233=
XR_002959730.1:n.784G>A
NR_110005.2:n.662G>A