Canonical Allele Identifier: CA2758856131

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149177899_149177900del , CM000665.2:g.149177899_149177900del	GRCh38
NC_000003.11:g.148895686_148895687del , CM000665.1:g.148895686_148895687del	GRCh37
NC_000003.10:g.150378376_150378377del	NCBI36
NG_011800.1:g.49146_49147del
NG_011800.2:g.49146_49147del
NG_011800.3:g.49146_49147del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2958_2959del MANE Select	ENSP00000264613.6:p.Met987GlyfsTer3
ENST00000264613.10:c.2958_2959del	ENSP00000264613.6:p.Met987GlyfsTer3
ENST00000460674.5:n.875_876del
ENST00000463556.5:n.480_481del
ENST00000473296.1:n.8_9del
ENST00000479771.5:c.363_364del	ENSP00000420367.1:p.Met122GlyfsTer3
ENST00000481169.5:c.2745_2746del	ENSP00000418773.1:p.Met916GlyfsTer3
ENST00000490639.5:n.2990_2991del
ENST00000494544.1:c.2307_2308del	ENSP00000420545.1:p.Met770GlyfsTer3
NM_000096.3:c.2958_2959del	NP_000087.1:p.Met987GlyfsTer3
NR_046371.1:n.2998_2999del
XM_006713499.2:c.2958_2959del	XP_006713562.1:p.Met987GlyfsTer3
XM_006713500.2:c.2958_2959del	XP_006713563.1:p.Met987GlyfsTer3
XM_006713501.2:c.2958_2959del	XP_006713564.1:p.Met987GlyfsTer3
XM_011512435.1:c.2958_2959del	XP_011510737.1:p.Met987GlyfsTer3
XR_427361.2:n.3216_3217del
XM_006713499.3:c.2958_2959del	XP_006713562.1:p.Met987GlyfsTer3
XM_006713500.4:c.2958_2959del	XP_006713563.1:p.Met987GlyfsTer3
XM_006713501.3:c.2958_2959del	XP_006713564.1:p.Met987GlyfsTer3
XM_011512435.2:c.2958_2959del	XP_011510737.1:p.Met987GlyfsTer3
XM_017005734.2:c.2958_2959del	XP_016861223.1:p.Met987GlyfsTer3
XM_017005735.2:c.2958_2959del	XP_016861224.1:p.Met987GlyfsTer3
XR_427361.3:n.3174_3175del
NM_000096.4:c.2958_2959del MANE Select	NP_000087.2:p.Met987GlyfsTer3
NR_046371.2:n.2782_2783del