Canonical Allele Identifier: CA354932784

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149188073G>A , CM000665.2:g.149188073G>A	GRCh38
NC_000003.11:g.148905860G>A , CM000665.1:g.148905860G>A	GRCh37
NC_000003.10:g.150388550G>A	NCBI36
NG_011800.1:g.38973C>T
NG_011800.2:g.38973C>T
NG_011800.3:g.38973C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000096.4:c.1843C>T MANE Select	NP_000087.2:p.Gln615Ter
ENST00000264613.11:c.1843C>T MANE Select	ENSP00000264613.6:p.Gln615Ter
NM_000096.3:c.1843C>T	NP_000087.1:p.Gln615Ter
NR_046371.1:n.2096C>T
NR_046371.2:n.1880C>T
ENST00000264613.10:c.1843C>T	ENSP00000264613.6:p.Gln615Ter
ENST00000462336.5:n.217C>T
ENST00000471356.1:n.662C>T
ENST00000481169.5:c.1843C>T	ENSP00000418773.1:p.Gln615Ter
ENST00000489736.5:n.1068C>T
ENST00000490639.5:n.1875C>T
ENST00000494544.1:c.1192C>T	ENSP00000420545.1:p.Gln398Ter
ENST00000497797.5:n.452C>T
ENST00000497902.5:n.24C>T
XM_006713499.2:c.1843C>T	XP_006713562.1:p.Gln615Ter
XM_006713499.3:c.1843C>T	XP_006713562.1:p.Gln615Ter
XM_006713500.2:c.1843C>T	XP_006713563.1:p.Gln615Ter
XM_006713500.4:c.1843C>T	XP_006713563.1:p.Gln615Ter
XM_006713501.2:c.1843C>T	XP_006713564.1:p.Gln615Ter
XM_006713501.3:c.1843C>T	XP_006713564.1:p.Gln615Ter
XM_006713502.2:c.1843C>T	XP_006713565.1:p.Gln615Ter
XM_011512435.1:c.1843C>T	XP_011510737.1:p.Gln615Ter
XM_011512435.2:c.1843C>T	XP_011510737.1:p.Gln615Ter
XM_017005734.2:c.1843C>T	XP_016861223.1:p.Gln615Ter
XM_017005735.2:c.1843C>T	XP_016861224.1:p.Gln615Ter
XR_427361.2:n.2101C>T
XR_427361.3:n.2059C>T