Canonical Allele Identifier: CA2668139210

Gene: CP

Linked Data

• gnomAD v4: 3-149186079-GTC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186083_149186084del , CM000665.2:g.149186083_149186084del	GRCh38
NC_000003.11:g.148903870_148903871del , CM000665.1:g.148903870_148903871del	GRCh37
NC_000003.10:g.150386560_150386561del	NCBI36
NG_011800.1:g.40965_40966del
NG_011800.2:g.40965_40966del
NG_011800.3:g.40965_40966del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2077+439_2077+440del MANE Select	ENSP00000264613.6:n.2077+439_2077+440del
ENST00000264613.10:c.2077+439_2077+440del	ENSP00000264613.6:n.2077+439_2077+440del
ENST00000462336.5:n.451+439_451+440del
ENST00000481169.5:c.1865-635_1865-634del	ENSP00000418773.1:n.1865-635_1865-634del
ENST00000489736.5:n.1741_1742del
ENST00000490639.5:n.2109+439_2109+440del
ENST00000494544.1:c.1426+439_1426+440del	ENSP00000420545.1:n.1426+439_1426+440del
ENST00000497902.5:n.258+439_258+440del
NM_000096.3:c.2077+439_2077+440del	NP_000087.1:n.2077+439_2077+440del
NR_046371.1:n.2118-635_2118-634del
XM_006713499.2:c.2077+439_2077+440del	XP_006713562.1:n.2077+439_2077+440del
XM_006713500.2:c.2077+439_2077+440del	XP_006713563.1:n.2077+439_2077+440del
XM_006713501.2:c.2077+439_2077+440del	XP_006713564.1:n.2077+439_2077+440del
XM_006713502.2:c.2077+439_2077+440del	XP_006713565.1:n.2077+439_2077+440del
XM_011512435.1:c.2077+439_2077+440del	XP_011510737.1:n.2077+439_2077+440del
XR_427361.2:n.2335+439_2335+440del
XM_006713499.3:c.2077+439_2077+440del	XP_006713562.1:n.2077+439_2077+440del
XM_006713500.4:c.2077+439_2077+440del	XP_006713563.1:n.2077+439_2077+440del
XM_006713501.3:c.2077+439_2077+440del	XP_006713564.1:n.2077+439_2077+440del
XM_011512435.2:c.2077+439_2077+440del	XP_011510737.1:n.2077+439_2077+440del
XM_017005734.2:c.2077+439_2077+440del	XP_016861223.1:n.2077+439_2077+440del
XM_017005735.2:c.2077+439_2077+440del	XP_016861224.1:n.2077+439_2077+440del
XR_427361.3:n.2293+439_2293+440del
NM_000096.4:c.2077+439_2077+440del MANE Select	NP_000087.2:n.2077+439_2077+440del
NR_046371.2:n.1902-635_1902-634del