Canonical Allele Identifier: CA354919383

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149212455A>C , CM000665.2:g.149212455A>C	GRCh38
NC_000003.11:g.148930242A>C , CM000665.1:g.148930242A>C	GRCh37
NC_000003.10:g.150412932A>C	NCBI36
NG_011800.1:g.14591T>G
NG_011800.2:g.14591T>G
NG_011800.3:g.14591T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000096.4:c.390T>G MANE Select	NP_000087.2:p.His130Gln
ENST00000264613.11:c.390T>G MANE Select	ENSP00000264613.6:p.His130Gln
NM_000096.3:c.390T>G	NP_000087.1:p.His130Gln
NR_046371.1:n.643T>G
NR_046371.2:n.427T>G
ENST00000264613.10:c.390T>G	ENSP00000264613.6:p.His130Gln
ENST00000455472.3:c.510T>G	ENSP00000426888.1:p.His170Gln
ENST00000481169.5:c.390T>G	ENSP00000418773.1:p.His130Gln
ENST00000490639.5:n.422T>G
XM_006713499.2:c.390T>G	XP_006713562.1:p.His130Gln
XM_006713499.3:c.390T>G	XP_006713562.1:p.His130Gln
XM_006713500.2:c.390T>G	XP_006713563.1:p.His130Gln
XM_006713500.4:c.390T>G	XP_006713563.1:p.His130Gln
XM_006713501.2:c.390T>G	XP_006713564.1:p.His130Gln
XM_006713501.3:c.390T>G	XP_006713564.1:p.His130Gln
XM_006713502.2:c.390T>G	XP_006713565.1:p.His130Gln
XM_011512435.1:c.390T>G	XP_011510737.1:p.His130Gln
XM_011512435.2:c.390T>G	XP_011510737.1:p.His130Gln
XM_017005734.2:c.390T>G	XP_016861223.1:p.His130Gln
XM_017005735.2:c.390T>G	XP_016861224.1:p.His130Gln
XR_427361.2:n.648T>G
XR_427361.3:n.606T>G