Canonical Allele Identifier: CA2668137692

Gene: CP

Linked Data

• gnomAD v4: 3-149181976-ACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149181977_149181978del , CM000665.2:g.149181977_149181978del	GRCh38
NC_000003.11:g.148899764_148899765del , CM000665.1:g.148899764_148899765del	GRCh37
NC_000003.10:g.150382454_150382455del	NCBI36
NG_011800.1:g.45068_45069del
NG_011800.2:g.45068_45069del
NG_011800.3:g.45068_45069del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2554+27_2554+28del MANE Select	ENSP00000264613.6:n.2554+27_2554+28del
ENST00000264613.10:c.2554+27_2554+28del	ENSP00000264613.6:n.2554+27_2554+28del
ENST00000481169.5:c.2341+27_2341+28del	ENSP00000418773.1:n.2341+27_2341+28del
ENST00000490639.5:n.2586+27_2586+28del
ENST00000494544.1:c.1903+27_1903+28del	ENSP00000420545.1:n.1903+27_1903+28del
NM_000096.3:c.2554+27_2554+28del	NP_000087.1:n.2554+27_2554+28del
NR_046371.1:n.2594+27_2594+28del
XM_006713499.2:c.2554+27_2554+28del	XP_006713562.1:n.2554+27_2554+28del
XM_006713500.2:c.2554+27_2554+28del	XP_006713563.1:n.2554+27_2554+28del
XM_006713501.2:c.2554+27_2554+28del	XP_006713564.1:n.2554+27_2554+28del
XM_006713502.2:c.2554+27_2554+28del	XP_006713565.1:n.2554+27_2554+28del
XM_011512435.1:c.2554+27_2554+28del	XP_011510737.1:n.2554+27_2554+28del
XR_427361.2:n.2812+27_2812+28del
XM_006713499.3:c.2554+27_2554+28del	XP_006713562.1:n.2554+27_2554+28del
XM_006713500.4:c.2554+27_2554+28del	XP_006713563.1:n.2554+27_2554+28del
XM_006713501.3:c.2554+27_2554+28del	XP_006713564.1:n.2554+27_2554+28del
XM_011512435.2:c.2554+27_2554+28del	XP_011510737.1:n.2554+27_2554+28del
XM_017005734.2:c.2554+27_2554+28del	XP_016861223.1:n.2554+27_2554+28del
XM_017005735.2:c.2554+27_2554+28del	XP_016861224.1:n.2554+27_2554+28del
XR_427361.3:n.2770+27_2770+28del
NM_000096.4:c.2554+27_2554+28del MANE Select	NP_000087.2:n.2554+27_2554+28del
NR_046371.2:n.2378+27_2378+28del