Canonical Allele Identifier: CA354931160

Gene: CP

Linked Data

• gnomAD v4: 3-149182121-T-C
• MyVariant Identifiers: chr3:g.148899908T>C (hg19) ; chr3:g.149182121T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149182121T>C , CM000665.2:g.149182121T>C	GRCh38
NC_000003.11:g.148899908T>C , CM000665.1:g.148899908T>C	GRCh37
NC_000003.10:g.150382598T>C	NCBI36
NG_011800.1:g.44925A>G
NG_011800.2:g.44925A>G
NG_011800.3:g.44925A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2438A>G MANE Select	ENSP00000264613.6:p.His813Arg
ENST00000264613.10:c.2438A>G	ENSP00000264613.6:p.His813Arg
ENST00000481169.5:c.2225A>G	ENSP00000418773.1:p.His742Arg
ENST00000490639.5:n.2470A>G
ENST00000494544.1:c.1787A>G	ENSP00000420545.1:p.His596Arg
NM_000096.3:c.2438A>G	NP_000087.1:p.His813Arg
NR_046371.1:n.2478A>G
XM_006713499.2:c.2438A>G	XP_006713562.1:p.His813Arg
XM_006713500.2:c.2438A>G	XP_006713563.1:p.His813Arg
XM_006713501.2:c.2438A>G	XP_006713564.1:p.His813Arg
XM_006713502.2:c.2438A>G	XP_006713565.1:p.His813Arg
XM_011512435.1:c.2438A>G	XP_011510737.1:p.His813Arg
XR_427361.2:n.2696A>G
XM_006713499.3:c.2438A>G	XP_006713562.1:p.His813Arg
XM_006713500.4:c.2438A>G	XP_006713563.1:p.His813Arg
XM_006713501.3:c.2438A>G	XP_006713564.1:p.His813Arg
XM_011512435.2:c.2438A>G	XP_011510737.1:p.His813Arg
XM_017005734.2:c.2438A>G	XP_016861223.1:p.His813Arg
XM_017005735.2:c.2438A>G	XP_016861224.1:p.His813Arg
XR_427361.3:n.2654A>G
NM_000096.4:c.2438A>G MANE Select	NP_000087.2:p.His813Arg
NR_046371.2:n.2262A>G