Canonical Allele Identifier: CA388462268
Gene: GPC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.91693742C>G , CM000675.2:g.91693742C>G GRCh38
NC_000013.10:g.92345996C>G , CM000675.1:g.92345996C>G GRCh37
NC_000013.9:g.91143997C>G NCBI36
NG_009370.1:g.300062C>G
NG_009370.2:g.300062C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000377067.9:c.881C>G MANE Select ENSP00000366267.3:p.Ala294Gly
ENST00000377067.8:c.881C>G ENSP00000366267.3:p.Ala294Gly
ENST00000618596.1:c.557C>G ENSP00000480819.1:p.Ala186Gly
NM_004466.5:c.881C>G NP_004457.1:p.Ala294Gly
XM_011521054.1:c.881C>G XP_011519356.1:p.Ala294Gly
XM_011521055.1:c.881C>G XP_011519357.1:p.Ala294Gly
XM_011521056.1:c.881C>G XP_011519358.1:p.Ala294Gly
XM_011521057.1:c.881C>G XP_011519359.1:p.Ala294Gly
XM_011521058.1:c.881C>G XP_011519360.1:p.Ala294Gly
XM_011521059.1:c.881C>G XP_011519361.1:p.Ala294Gly
XM_011521060.1:c.881C>G XP_011519362.1:p.Ala294Gly
XM_011521054.3:c.881C>G XP_011519356.1:p.Ala294Gly
XM_011521055.3:c.881C>G XP_011519357.1:p.Ala294Gly
XM_011521056.3:c.881C>G XP_011519358.1:p.Ala294Gly
XM_011521057.3:c.881C>G XP_011519359.1:p.Ala294Gly
XM_011521058.2:c.881C>G XP_011519360.1:p.Ala294Gly
XM_011521059.2:c.881C>G XP_011519361.1:p.Ala294Gly
XM_011521060.2:c.881C>G XP_011519362.1:p.Ala294Gly
XM_017020435.2:c.881C>G XP_016875924.1:p.Ala294Gly
XM_017020436.2:c.881C>G XP_016875925.1:p.Ala294Gly
XM_017020437.1:c.881C>G XP_016875926.1:p.Ala294Gly
NM_004466.6:c.881C>G MANE Select NP_004457.1:p.Ala294Gly