Canonical Allele Identifier: CA2661134

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149206245G>A , CM000665.2:g.149206245G>A	GRCh38
NC_000003.11:g.148924032G>A , CM000665.1:g.148924032G>A	GRCh37
NC_000003.10:g.150406722G>A	NCBI36
NG_011800.1:g.20801C>T
NG_011800.2:g.20801C>T
NG_011800.3:g.20801C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000096.4:c.1131C>T MANE Select	NP_000087.2:p.Ala377=
ENST00000264613.11:c.1131C>T MANE Select	ENSP00000264613.6:p.Ala377=
NM_000096.3:c.1131C>T	NP_000087.1:p.Ala377=
NR_046371.1:n.1384C>T
NR_046371.2:n.1168C>T
ENST00000264613.10:c.1131C>T	ENSP00000264613.6:p.Ala377=
ENST00000481169.5:c.1131C>T	ENSP00000418773.1:p.Ala377=
ENST00000489736.5:n.356C>T
ENST00000490639.5:n.1163C>T
ENST00000494544.1:c.480C>T	ENSP00000420545.1:p.Ala160=
XM_006713499.2:c.1131C>T	XP_006713562.1:p.Ala377=
XM_006713499.3:c.1131C>T	XP_006713562.1:p.Ala377=
XM_006713500.2:c.1131C>T	XP_006713563.1:p.Ala377=
XM_006713500.4:c.1131C>T	XP_006713563.1:p.Ala377=
XM_006713501.2:c.1131C>T	XP_006713564.1:p.Ala377=
XM_006713501.3:c.1131C>T	XP_006713564.1:p.Ala377=
XM_006713502.2:c.1131C>T	XP_006713565.1:p.Ala377=
XM_011512435.1:c.1131C>T	XP_011510737.1:p.Ala377=
XM_011512435.2:c.1131C>T	XP_011510737.1:p.Ala377=
XM_017005734.2:c.1131C>T	XP_016861223.1:p.Ala377=
XM_017005735.2:c.1131C>T	XP_016861224.1:p.Ala377=
XR_427361.2:n.1389C>T
XR_427361.3:n.1347C>T