Canonical Allele Identifier: CA2660742

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149182037G>C , CM000665.2:g.149182037G>C	GRCh38
NC_000003.11:g.148899824G>C , CM000665.1:g.148899824G>C	GRCh37
NC_000003.10:g.150382514G>C	NCBI36
NG_011800.1:g.45009C>G
NG_011800.2:g.45009C>G
NG_011800.3:g.45009C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000096.4:c.2522C>G MANE Select	NP_000087.2:p.Thr841Arg
ENST00000264613.11:c.2522C>G MANE Select	ENSP00000264613.6:p.Thr841Arg
NM_000096.3:c.2522C>G	NP_000087.1:p.Thr841Arg
NR_046371.1:n.2562C>G
NR_046371.2:n.2346C>G
ENST00000264613.10:c.2522C>G	ENSP00000264613.6:p.Thr841Arg
ENST00000481169.5:c.2309C>G	ENSP00000418773.1:p.Thr770Arg
ENST00000490639.5:n.2554C>G
ENST00000494544.1:c.1871C>G	ENSP00000420545.1:p.Thr624Arg
XM_006713499.2:c.2522C>G	XP_006713562.1:p.Thr841Arg
XM_006713499.3:c.2522C>G	XP_006713562.1:p.Thr841Arg
XM_006713500.2:c.2522C>G	XP_006713563.1:p.Thr841Arg
XM_006713500.4:c.2522C>G	XP_006713563.1:p.Thr841Arg
XM_006713501.2:c.2522C>G	XP_006713564.1:p.Thr841Arg
XM_006713501.3:c.2522C>G	XP_006713564.1:p.Thr841Arg
XM_006713502.2:c.2522C>G	XP_006713565.1:p.Thr841Arg
XM_011512435.1:c.2522C>G	XP_011510737.1:p.Thr841Arg
XM_011512435.2:c.2522C>G	XP_011510737.1:p.Thr841Arg
XM_017005734.2:c.2522C>G	XP_016861223.1:p.Thr841Arg
XM_017005735.2:c.2522C>G	XP_016861224.1:p.Thr841Arg
XR_427361.2:n.2780C>G
XR_427361.3:n.2738C>G