Canonical Allele Identifier: CA2668137684

Gene: CP

Linked Data

• gnomAD v4: 3-149181976-A-ACCCCCCCCCCCCCCCCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149181978_149181979insCCCCCCCCCCCCCCCCCC , CM000665.2:g.149181978_149181979insCCCCCCCCCCCCCCCCCC	GRCh38
NC_000003.11:g.148899765_148899766insCCCCCCCCCCCCCCCCCC , CM000665.1:g.148899765_148899766insCCCCCCCCCCCCCCCCCC	GRCh37
NC_000003.10:g.150382455_150382456insCCCCCCCCCCCCCCCCCC	NCBI36
NG_011800.1:g.45069_45070insGGGGGGGGGGGGGGGGGG
NG_011800.2:g.45069_45070insGGGGGGGGGGGGGGGGGG
NG_011800.3:g.45069_45070insGGGGGGGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2554+28_2554+29insGGGGGGGGGGGGGGGGGG MANE Select	ENSP00000264613.6:n.2554+28_2554+29insGGGGGGGGGGGGGGGGGG
ENST00000264613.10:c.2554+28_2554+29insGGGGGGGGGGGGGGGGGG	ENSP00000264613.6:n.2554+28_2554+29insGGGGGGGGGGGGGGGGGG
ENST00000481169.5:c.2341+28_2341+29insGGGGGGGGGGGGGGGGGG	ENSP00000418773.1:n.2341+28_2341+29insGGGGGGGGGGGGGGGGGG
ENST00000490639.5:n.2586+28_2586+29insGGGGGGGGGGGGGGGGGG
ENST00000494544.1:c.1903+28_1903+29insGGGGGGGGGGGGGGGGGG	ENSP00000420545.1:n.1903+28_1903+29insGGGGGGGGGGGGGGGGGG
NM_000096.3:c.2554+28_2554+29insGGGGGGGGGGGGGGGGGG	NP_000087.1:n.2554+28_2554+29insGGGGGGGGGGGGGGGGGG
NR_046371.1:n.2594+28_2594+29insGGGGGGGGGGGGGGGGGG
XM_006713499.2:c.2554+28_2554+29insGGGGGGGGGGGGGGGGGG	XP_006713562.1:n.2554+28_2554+29insGGGGGGGGGGGGGGGGGG
XM_006713500.2:c.2554+28_2554+29insGGGGGGGGGGGGGGGGGG	XP_006713563.1:n.2554+28_2554+29insGGGGGGGGGGGGGGGGGG
XM_006713501.2:c.2554+28_2554+29insGGGGGGGGGGGGGGGGGG	XP_006713564.1:n.2554+28_2554+29insGGGGGGGGGGGGGGGGGG
XM_006713502.2:c.2554+28_2554+29insGGGGGGGGGGGGGGGGGG	XP_006713565.1:n.2554+28_2554+29insGGGGGGGGGGGGGGGGGG
XM_011512435.1:c.2554+28_2554+29insGGGGGGGGGGGGGGGGGG	XP_011510737.1:n.2554+28_2554+29insGGGGGGGGGGGGGGGGGG
XR_427361.2:n.2812+28_2812+29insGGGGGGGGGGGGGGGGGG
XM_006713499.3:c.2554+28_2554+29insGGGGGGGGGGGGGGGGGG	XP_006713562.1:n.2554+28_2554+29insGGGGGGGGGGGGGGGGGG
XM_006713500.4:c.2554+28_2554+29insGGGGGGGGGGGGGGGGGG	XP_006713563.1:n.2554+28_2554+29insGGGGGGGGGGGGGGGGGG
XM_006713501.3:c.2554+28_2554+29insGGGGGGGGGGGGGGGGGG	XP_006713564.1:n.2554+28_2554+29insGGGGGGGGGGGGGGGGGG
XM_011512435.2:c.2554+28_2554+29insGGGGGGGGGGGGGGGGGG	XP_011510737.1:n.2554+28_2554+29insGGGGGGGGGGGGGGGGGG
XM_017005734.2:c.2554+28_2554+29insGGGGGGGGGGGGGGGGGG	XP_016861223.1:n.2554+28_2554+29insGGGGGGGGGGGGGGGGGG
XM_017005735.2:c.2554+28_2554+29insGGGGGGGGGGGGGGGGGG	XP_016861224.1:n.2554+28_2554+29insGGGGGGGGGGGGGGGGGG
XR_427361.3:n.2770+28_2770+29insGGGGGGGGGGGGGGGGGG
NM_000096.4:c.2554+28_2554+29insGGGGGGGGGGGGGGGGGG MANE Select	NP_000087.2:n.2554+28_2554+29insGGGGGGGGGGGGGGGGGG
NR_046371.2:n.2378+28_2378+29insGGGGGGGGGGGGGGGGGG