Canonical Allele Identifier: CA356112839
Gene: LRPAP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.3519812C>T (hg19) chr4:g.3518085C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3518085C>T , CM000666.2:g.3518085C>T GRCh38
NC_000004.11:g.3519812C>T , CM000666.1:g.3519812C>T GRCh37
NC_000004.10:g.3489610C>T NCBI36
NG_033873.1:g.19413G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000648517.1:c.700G>A ENSP00000496947.1:p.Gly234Ser
ENST00000650182.1:c.700G>A MANE Select ENSP00000497444.1:p.Gly234Ser
ENST00000296325.9:n.663G>A
ENST00000500728.2:c.700G>A ENSP00000421922.1:p.Gly234Ser
ENST00000509198.1:n.746G>A
ENST00000515119.5:c.*477G>A ENSP00000421648.1:n.*477G>A
NM_002337.3:c.700G>A NP_002328.1:p.Gly234Ser
NR_110005.1:n.663G>A
NM_002337.4:c.700G>A MANE Select NP_002328.1:p.Gly234Ser
XR_002959730.1:n.785G>A
NR_110005.2:n.663G>A
Search 100 bp 5'
Search 100 bp 3'