Canonical Allele Identifier: CA1356029887

Gene: CRTAP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33114566C= , CM000665.2:g.33114566C=	GRCh38
NC_000003.11:g.33156058C= , CM000665.1:g.33156058C=	GRCh37
NC_000003.10:g.33131062C=	NCBI36
NG_008122.1:g.5609C= , LRG_4:g.5609C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320954.11:c.471+18C= MANE Select	ENSP00000323696.5:n.471+18C=
ENST00000320954.10:c.471+18C=	ENSP00000323696.5:n.471+18C=
ENST00000449224.1:c.471+18C=	ENSP00000409997.1:n.471+18C=
NM_006371.4:c.471+18C= , LRG_4t1:c.471+18C=	NP_006362.1:n.471+18C=
NM_006371.5:c.471+18C= MANE Select	NP_006362.1:n.471+18C=
NM_001393363.1:c.471+18C=	NP_001380292.1:n.471+18C=
NM_001393364.1:c.471+18C=	NP_001380293.1:n.471+18C=
NM_001393365.1:c.471+18C=	NP_001380294.1:n.471+18C=