Canonical Allele Identifier: CA1356029750
Gene: CRTAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33114361A= , CM000665.2:g.33114361A= GRCh38
NC_000003.11:g.33155853A= , CM000665.1:g.33155853A= GRCh37
NC_000003.10:g.33130857A= NCBI36
NG_008122.1:g.5404A= , LRG_4:g.5404A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320954.11:c.284A= MANE Select ENSP00000323696.5:p.Glu95=
ENST00000320954.10:c.284A= ENSP00000323696.5:p.Glu95=
ENST00000449224.1:c.284A= ENSP00000409997.1:p.Glu95=
NM_006371.4:c.284A= , LRG_4t1:c.284A= NP_006362.1:p.Glu95=
NM_006371.5:c.284A= MANE Select NP_006362.1:p.Glu95=
NM_001393363.1:c.284A= NP_001380292.1:p.Glu95=
NM_001393364.1:c.284A= NP_001380293.1:p.Glu95=
NM_001393365.1:c.284A= NP_001380294.1:p.Glu95=