Canonical Allele Identifier: CA1356029716

Gene: CRTAP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33114304T= , CM000665.2:g.33114304T=	GRCh38
NC_000003.11:g.33155796T= , CM000665.1:g.33155796T=	GRCh37
NC_000003.10:g.33130800T=	NCBI36
NG_008122.1:g.5347T= , LRG_4:g.5347T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320954.11:c.227T= MANE Select	ENSP00000323696.5:p.Leu76=
ENST00000320954.10:c.227T=	ENSP00000323696.5:p.Leu76=
ENST00000449224.1:c.227T=	ENSP00000409997.1:p.Leu76=
NM_006371.4:c.227T= , LRG_4t1:c.227T=	NP_006362.1:p.Leu76=
NM_006371.5:c.227T= MANE Select	NP_006362.1:p.Leu76=
NM_001393363.1:c.227T=	NP_001380292.1:p.Leu76=
NM_001393364.1:c.227T=	NP_001380293.1:p.Leu76=
NM_001393365.1:c.227T=	NP_001380294.1:p.Leu76=