Canonical Allele Identifier: CA2580615992

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149182048_149182056del , CM000665.2:g.149182048_149182056del	GRCh38
NC_000003.11:g.148899835_148899843del , CM000665.1:g.148899835_148899843del	GRCh37
NC_000003.10:g.150382525_150382533del	NCBI36
NG_011800.1:g.44990_44998del
NG_011800.2:g.44990_44998del
NG_011800.3:g.44990_44998del

Transcript Alleles

HGVS	Amino-acid Change
NM_000096.4:c.2503_2511del MANE Select	NP_000087.2:p.His835_His837del
ENST00000264613.11:c.2503_2511del MANE Select	ENSP00000264613.6:p.His835_His837del
NM_000096.3:c.2503_2511del	NP_000087.1:p.His835_His837del
NR_046371.1:n.2543_2551del
NR_046371.2:n.2327_2335del
ENST00000264613.10:c.2503_2511del	ENSP00000264613.6:p.His835_His837del
ENST00000481169.5:c.2290_2298del	ENSP00000418773.1:p.His764_His766del
ENST00000490639.5:n.2535_2543del
ENST00000494544.1:c.1852_1860del	ENSP00000420545.1:p.His618_His620del
XM_006713499.2:c.2503_2511del	XP_006713562.1:p.His835_His837del
XM_006713499.3:c.2503_2511del	XP_006713562.1:p.His835_His837del
XM_006713500.2:c.2503_2511del	XP_006713563.1:p.His835_His837del
XM_006713500.4:c.2503_2511del	XP_006713563.1:p.His835_His837del
XM_006713501.2:c.2503_2511del	XP_006713564.1:p.His835_His837del
XM_006713501.3:c.2503_2511del	XP_006713564.1:p.His835_His837del
XM_006713502.2:c.2503_2511del	XP_006713565.1:p.His835_His837del
XM_011512435.1:c.2503_2511del	XP_011510737.1:p.His835_His837del
XM_011512435.2:c.2503_2511del	XP_011510737.1:p.His835_His837del
XM_017005734.2:c.2503_2511del	XP_016861223.1:p.His835_His837del
XM_017005735.2:c.2503_2511del	XP_016861224.1:p.His835_His837del
XR_427361.2:n.2761_2769del
XR_427361.3:n.2719_2727del