Canonical Allele Identifier: CA356112852
Gene: LRPAP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.3519817T>C (hg19) chr4:g.3518090T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.3518090T>C , CM000666.2:g.3518090T>C GRCh38
NC_000004.11:g.3519817T>C , CM000666.1:g.3519817T>C GRCh37
NC_000004.10:g.3489615T>C NCBI36
NG_033873.1:g.19408A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000648517.1:c.695A>G ENSP00000496947.1:p.Asn232Ser
ENST00000650182.1:c.695A>G MANE Select ENSP00000497444.1:p.Asn232Ser
ENST00000296325.9:n.658A>G
ENST00000500728.2:c.695A>G ENSP00000421922.1:p.Asn232Ser
ENST00000509198.1:n.741A>G
ENST00000515119.5:c.*472A>G ENSP00000421648.1:n.*472A>G
NM_002337.3:c.695A>G NP_002328.1:p.Asn232Ser
NR_110005.1:n.658A>G
NM_002337.4:c.695A>G MANE Select NP_002328.1:p.Asn232Ser
XR_002959730.1:n.780A>G
NR_110005.2:n.658A>G
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