Canonical Allele Identifier: CA2504092837

Gene: CRTAP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.33114567_33114568insCCACACCACGCCCCTTAGCTAAGGGTCCC , CM000665.2:g.33114567_33114568insCCACACCACGCCCCTTAGCTAAGGGTCCC	GRCh38
NC_000003.11:g.33156059_33156060insCCACACCACGCCCCTTAGCTAAGGGTCCC , CM000665.1:g.33156059_33156060insCCACACCACGCCCCTTAGCTAAGGGTCCC	GRCh37
NC_000003.10:g.33131063_33131064insCCACACCACGCCCCTTAGCTAAGGGTCCC	NCBI36
NG_008122.1:g.5610_5611insCCACACCACGCCCCTTAGCTAAGGGTCCC , LRG_4:g.5610_5611insCCACACCACGCCCCTTAGCTAAGGGTCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320954.11:c.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGGTCCC MANE Select	ENSP00000323696.5:n.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGG...
ENST00000320954.10:c.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGGTCCC	ENSP00000323696.5:n.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGG...
ENST00000449224.1:c.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGGTCCC	ENSP00000409997.1:n.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGG...
NM_006371.4:c.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGGTCCC , LRG_4t1:c.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGGTCCC	NP_006362.1:n.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGGTCCC
NM_006371.5:c.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGGTCCC MANE Select	NP_006362.1:n.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGGTCCC
NM_001393363.1:c.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGGTCCC	NP_001380292.1:n.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGGTCC...
NM_001393364.1:c.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGGTCCC	NP_001380293.1:n.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGGTCC...
NM_001393365.1:c.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGGTCCC	NP_001380294.1:n.471+19_471+20insCCACACCACGCCCCTTAGCTAAGGGTCC...