Canonical Allele Identifier: CA390414224
Community Standard Title: NM_019589.3(YLPM1):c.2537A>G (p.Gln846Arg)
Gene: YLPM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.74797834A>G , CM000676.2:g.74797834A>G GRCh38
NC_000014.8:g.75264537A>G , CM000676.1:g.75264537A>G GRCh37
NC_000014.7:g.74334290A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_019589.3:c.2537A>G MANE Select NP_062535.2:p.Gln846Arg
ENST00000325680.12:c.2537A>G MANE Select ENSP00000324463.7:p.Gln846Arg
NM_019589.2:c.2537A>G NP_062535.2:p.Gln846Arg
ENST00000325680.11:c.2537A>G ENSP00000324463.7:p.Gln846Arg
ENST00000549293.5:c.1196A>G ENSP00000449860.1:p.Gln399Arg
ENST00000552421.5:c.2283-4722A>G ENSP00000447921.1:n.2283-4722A>G
XM_005267860.3:c.2537A>G XP_005267917.1:p.Gln846Arg
XM_005267860.4:c.2537A>G XP_005267917.1:p.Gln846Arg
XM_011536966.1:c.1322A>G XP_011535268.1:p.Gln441Arg
XM_011536966.2:c.1322A>G XP_011535268.1:p.Gln441Arg
XM_011536967.1:c.2283-4722A>G XP_011535269.1:n.2283-4722A>G
XM_011536967.2:c.2283-4722A>G XP_011535269.1:n.2283-4722A>G
XR_001750436.2:n.2711A>G
XR_943494.1:n.2705A>G