Canonical Allele Identifier: CA546941793

Gene: CP

Linked Data

• dbSNP Id: rs1342413555
• gnomAD v2: 3-148904124-A-AT
• gnomAD v3: 3-149186337-A-AT
• gnomAD v4: 3-149186337-A-AT
• MyVariant Identifiers: chr3:g.148904124_148904125insT (hg19) ; chr3:g.149186337_149186338insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186337_149186338insT , CM000665.2:g.149186337_149186338insT	GRCh38
NC_000003.11:g.148904124_148904125insT , CM000665.1:g.148904124_148904125insT	GRCh37
NC_000003.10:g.150386814_150386815insT	NCBI36
NG_011800.1:g.40708_40709insA
NG_011800.2:g.40708_40709insA
NG_011800.3:g.40708_40709insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2077+182_2077+183insA MANE Select	ENSP00000264613.6:n.2077+182_2077+183insA
ENST00000264613.10:c.2077+182_2077+183insA	ENSP00000264613.6:n.2077+182_2077+183insA
ENST00000462336.5:n.451+182_451+183insA
ENST00000481169.5:c.1865-892_1865-891insA	ENSP00000418773.1:n.1865-892_1865-891insA
ENST00000489736.5:n.1484_1485insA
ENST00000490639.5:n.2109+182_2109+183insA
ENST00000494544.1:c.1426+182_1426+183insA	ENSP00000420545.1:n.1426+182_1426+183insA
ENST00000497902.5:n.258+182_258+183insA
NM_000096.3:c.2077+182_2077+183insA	NP_000087.1:n.2077+182_2077+183insA
NR_046371.1:n.2118-892_2118-891insA
XM_006713499.2:c.2077+182_2077+183insA	XP_006713562.1:n.2077+182_2077+183insA
XM_006713500.2:c.2077+182_2077+183insA	XP_006713563.1:n.2077+182_2077+183insA
XM_006713501.2:c.2077+182_2077+183insA	XP_006713564.1:n.2077+182_2077+183insA
XM_006713502.2:c.2077+182_2077+183insA	XP_006713565.1:n.2077+182_2077+183insA
XM_011512435.1:c.2077+182_2077+183insA	XP_011510737.1:n.2077+182_2077+183insA
XR_427361.2:n.2335+182_2335+183insA
XM_006713499.3:c.2077+182_2077+183insA	XP_006713562.1:n.2077+182_2077+183insA
XM_006713500.4:c.2077+182_2077+183insA	XP_006713563.1:n.2077+182_2077+183insA
XM_006713501.3:c.2077+182_2077+183insA	XP_006713564.1:n.2077+182_2077+183insA
XM_011512435.2:c.2077+182_2077+183insA	XP_011510737.1:n.2077+182_2077+183insA
XM_017005734.2:c.2077+182_2077+183insA	XP_016861223.1:n.2077+182_2077+183insA
XM_017005735.2:c.2077+182_2077+183insA	XP_016861224.1:n.2077+182_2077+183insA
XR_427361.3:n.2293+182_2293+183insA
NM_000096.4:c.2077+182_2077+183insA MANE Select	NP_000087.2:n.2077+182_2077+183insA
NR_046371.2:n.1902-892_1902-891insA