Canonical Allele Identifier: CA2660748

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149182061G>C , CM000665.2:g.149182061G>C	GRCh38
NC_000003.11:g.148899848G>C , CM000665.1:g.148899848G>C	GRCh37
NC_000003.10:g.150382538G>C	NCBI36
NG_011800.1:g.44985C>G
NG_011800.2:g.44985C>G
NG_011800.3:g.44985C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000096.4:c.2498C>G MANE Select	NP_000087.2:p.Ser833Ter
ENST00000264613.11:c.2498C>G MANE Select	ENSP00000264613.6:p.Ser833Ter
NM_000096.3:c.2498C>G	NP_000087.1:p.Ser833Ter
NR_046371.1:n.2538C>G
NR_046371.2:n.2322C>G
ENST00000264613.10:c.2498C>G	ENSP00000264613.6:p.Ser833Ter
ENST00000481169.5:c.2285C>G	ENSP00000418773.1:p.Ser762Ter
ENST00000490639.5:n.2530C>G
ENST00000494544.1:c.1847C>G	ENSP00000420545.1:p.Ser616Ter
XM_006713499.2:c.2498C>G	XP_006713562.1:p.Ser833Ter
XM_006713499.3:c.2498C>G	XP_006713562.1:p.Ser833Ter
XM_006713500.2:c.2498C>G	XP_006713563.1:p.Ser833Ter
XM_006713500.4:c.2498C>G	XP_006713563.1:p.Ser833Ter
XM_006713501.2:c.2498C>G	XP_006713564.1:p.Ser833Ter
XM_006713501.3:c.2498C>G	XP_006713564.1:p.Ser833Ter
XM_006713502.2:c.2498C>G	XP_006713565.1:p.Ser833Ter
XM_011512435.1:c.2498C>G	XP_011510737.1:p.Ser833Ter
XM_011512435.2:c.2498C>G	XP_011510737.1:p.Ser833Ter
XM_017005734.2:c.2498C>G	XP_016861223.1:p.Ser833Ter
XM_017005735.2:c.2498C>G	XP_016861224.1:p.Ser833Ter
XR_427361.2:n.2756C>G
XR_427361.3:n.2714C>G