Canonical Allele Identifier: CA2668139237

Gene: CP

Linked Data

• gnomAD v4: 3-149186108-G-GTGTAGATCTCGGTGGTCGCCGTAT

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186108_149186109insTGTAGATCTCGGTGGTCGCCGTAT , CM000665.2:g.149186108_149186109insTGTAGATCTCGGTGGTCGCCGTAT	GRCh38
NC_000003.11:g.148903895_148903896insTGTAGATCTCGGTGGTCGCCGTAT , CM000665.1:g.148903895_148903896insTGTAGATCTCGGTGGTCGCCGTAT	GRCh37
NC_000003.10:g.150386585_150386586insTGTAGATCTCGGTGGTCGCCGTAT	NCBI36
NG_011800.1:g.40937_40938insATACGGCGACCACCGAGATCTACA
NG_011800.2:g.40937_40938insATACGGCGACCACCGAGATCTACA
NG_011800.3:g.40937_40938insATACGGCGACCACCGAGATCTACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2077+411_2077+412insATACGGCGACCACCGAGATCTACA MANE Select	ENSP00000264613.6:n.2077+411_2077+412insATACGGCGACCACCGAGATCT...
ENST00000264613.10:c.2077+411_2077+412insATACGGCGACCACCGAGATCTACA	ENSP00000264613.6:n.2077+411_2077+412insATACGGCGACCACCGAGATCT...
ENST00000462336.5:n.451+411_451+412insATACGGCGACCACCGAGATCTACA
ENST00000481169.5:c.1865-663_1865-662insATACGGCGACCACCGAGATCTACA	ENSP00000418773.1:n.1865-663_1865-662insATACGGCGACCACCGAGATCT...
ENST00000489736.5:n.1713_1714insATACGGCGACCACCGAGATCTACA
ENST00000490639.5:n.2109+411_2109+412insATACGGCGACCACCGAGATCTACA
ENST00000494544.1:c.1426+411_1426+412insATACGGCGACCACCGAGATCTACA	ENSP00000420545.1:n.1426+411_1426+412insATACGGCGACCACCGAGATCT...
ENST00000497902.5:n.258+411_258+412insATACGGCGACCACCGAGATCTACA
NM_000096.3:c.2077+411_2077+412insATACGGCGACCACCGAGATCTACA	NP_000087.1:n.2077+411_2077+412insATACGGCGACCACCGAGATCTACA
NR_046371.1:n.2118-663_2118-662insATACGGCGACCACCGAGATCTACA
XM_006713499.2:c.2077+411_2077+412insATACGGCGACCACCGAGATCTACA	XP_006713562.1:n.2077+411_2077+412insATACGGCGACCACCGAGATCTACA...
XM_006713500.2:c.2077+411_2077+412insATACGGCGACCACCGAGATCTACA	XP_006713563.1:n.2077+411_2077+412insATACGGCGACCACCGAGATCTACA...
XM_006713501.2:c.2077+411_2077+412insATACGGCGACCACCGAGATCTACA	XP_006713564.1:n.2077+411_2077+412insATACGGCGACCACCGAGATCTACA...
XM_006713502.2:c.2077+411_2077+412insATACGGCGACCACCGAGATCTACA	XP_006713565.1:n.2077+411_2077+412insATACGGCGACCACCGAGATCTACA...
XM_011512435.1:c.2077+411_2077+412insATACGGCGACCACCGAGATCTACA	XP_011510737.1:n.2077+411_2077+412insATACGGCGACCACCGAGATCTACA...
XR_427361.2:n.2335+411_2335+412insATACGGCGACCACCGAGATCTACA
XM_006713499.3:c.2077+411_2077+412insATACGGCGACCACCGAGATCTACA	XP_006713562.1:n.2077+411_2077+412insATACGGCGACCACCGAGATCTACA...
XM_006713500.4:c.2077+411_2077+412insATACGGCGACCACCGAGATCTACA	XP_006713563.1:n.2077+411_2077+412insATACGGCGACCACCGAGATCTACA...
XM_006713501.3:c.2077+411_2077+412insATACGGCGACCACCGAGATCTACA	XP_006713564.1:n.2077+411_2077+412insATACGGCGACCACCGAGATCTACA...
XM_011512435.2:c.2077+411_2077+412insATACGGCGACCACCGAGATCTACA	XP_011510737.1:n.2077+411_2077+412insATACGGCGACCACCGAGATCTACA...
XM_017005734.2:c.2077+411_2077+412insATACGGCGACCACCGAGATCTACA	XP_016861223.1:n.2077+411_2077+412insATACGGCGACCACCGAGATCTACA...
XM_017005735.2:c.2077+411_2077+412insATACGGCGACCACCGAGATCTACA	XP_016861224.1:n.2077+411_2077+412insATACGGCGACCACCGAGATCTACA...
XR_427361.3:n.2293+411_2293+412insATACGGCGACCACCGAGATCTACA
NM_000096.4:c.2077+411_2077+412insATACGGCGACCACCGAGATCTACA MANE Select	NP_000087.2:n.2077+411_2077+412insATACGGCGACCACCGAGATCTACA
NR_046371.2:n.1902-663_1902-662insATACGGCGACCACCGAGATCTACA