Canonical Allele Identifier: CA2668138251

Gene: CP

Linked Data

• gnomAD v4: 3-149182190-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149182190G>T , CM000665.2:g.149182190G>T	GRCh38
NC_000003.11:g.148899977G>T , CM000665.1:g.148899977G>T	GRCh37
NC_000003.10:g.150382667G>T	NCBI36
NG_011800.1:g.44856C>A
NG_011800.2:g.44856C>A
NG_011800.3:g.44856C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2426-57C>A MANE Select	ENSP00000264613.6:n.2426-57C>A
ENST00000264613.10:c.2426-57C>A	ENSP00000264613.6:n.2426-57C>A
ENST00000481169.5:c.2213-57C>A	ENSP00000418773.1:n.2213-57C>A
ENST00000490639.5:n.2458-57C>A
ENST00000494544.1:c.1775-57C>A	ENSP00000420545.1:n.1775-57C>A
NM_000096.3:c.2426-57C>A	NP_000087.1:n.2426-57C>A
NR_046371.1:n.2466-57C>A
XM_006713499.2:c.2426-57C>A	XP_006713562.1:n.2426-57C>A
XM_006713500.2:c.2426-57C>A	XP_006713563.1:n.2426-57C>A
XM_006713501.2:c.2426-57C>A	XP_006713564.1:n.2426-57C>A
XM_006713502.2:c.2426-57C>A	XP_006713565.1:n.2426-57C>A
XM_011512435.1:c.2426-57C>A	XP_011510737.1:n.2426-57C>A
XR_427361.2:n.2684-57C>A
XM_006713499.3:c.2426-57C>A	XP_006713562.1:n.2426-57C>A
XM_006713500.4:c.2426-57C>A	XP_006713563.1:n.2426-57C>A
XM_006713501.3:c.2426-57C>A	XP_006713564.1:n.2426-57C>A
XM_011512435.2:c.2426-57C>A	XP_011510737.1:n.2426-57C>A
XM_017005734.2:c.2426-57C>A	XP_016861223.1:n.2426-57C>A
XM_017005735.2:c.2426-57C>A	XP_016861224.1:n.2426-57C>A
XR_427361.3:n.2642-57C>A
NM_000096.4:c.2426-57C>A MANE Select	NP_000087.2:n.2426-57C>A
NR_046371.2:n.2250-57C>A