Canonical Allele Identifier: CA2660840

Gene: CP

Linked Data

• dbSNP Id: rs766920588
• ExAC: 3:148904257 C / CA
• gnomAD v2: 3-148904257-C-CA
• gnomAD v3: 3-149186470-C-CA
• gnomAD v4: 3-149186470-C-CA
• MyVariant Identifiers: chr3:g.148904257_148904258insA (hg19) ; chr3:g.149186470_149186471insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186474dup , CM000665.2:g.149186474dup	GRCh38
NC_000003.11:g.148904261dup , CM000665.1:g.148904261dup	GRCh37
NC_000003.10:g.150386951dup	NCBI36
NG_011800.1:g.40575dup
NG_011800.2:g.40575dup
NG_011800.3:g.40575dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2077+49dup MANE Select	ENSP00000264613.6:n.2077+49dup
ENST00000264613.10:c.2077+49dup	ENSP00000264613.6:n.2077+49dup
ENST00000462336.5:n.451+49dup
ENST00000481169.5:c.1865-1025dup	ENSP00000418773.1:n.1865-1025dup
ENST00000489736.5:n.1351dup
ENST00000490639.5:n.2109+49dup
ENST00000494544.1:c.1426+49dup	ENSP00000420545.1:n.1426+49dup
ENST00000497902.5:n.258+49dup
NM_000096.3:c.2077+49dup	NP_000087.1:n.2077+49dup
NR_046371.1:n.2118-1025dup
XM_006713499.2:c.2077+49dup	XP_006713562.1:n.2077+49dup
XM_006713500.2:c.2077+49dup	XP_006713563.1:n.2077+49dup
XM_006713501.2:c.2077+49dup	XP_006713564.1:n.2077+49dup
XM_006713502.2:c.2077+49dup	XP_006713565.1:n.2077+49dup
XM_011512435.1:c.2077+49dup	XP_011510737.1:n.2077+49dup
XR_427361.2:n.2335+49dup
XM_006713499.3:c.2077+49dup	XP_006713562.1:n.2077+49dup
XM_006713500.4:c.2077+49dup	XP_006713563.1:n.2077+49dup
XM_006713501.3:c.2077+49dup	XP_006713564.1:n.2077+49dup
XM_011512435.2:c.2077+49dup	XP_011510737.1:n.2077+49dup
XM_017005734.2:c.2077+49dup	XP_016861223.1:n.2077+49dup
XM_017005735.2:c.2077+49dup	XP_016861224.1:n.2077+49dup
XR_427361.3:n.2293+49dup
NM_000096.4:c.2077+49dup MANE Select	NP_000087.2:n.2077+49dup
NR_046371.2:n.1902-1025dup