Canonical Allele Identifier: CA2543962058

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149195267A>G , CM000665.2:g.149195267A>G	GRCh38
NC_000003.11:g.148913054A>G , CM000665.1:g.148913054A>G	GRCh37
NC_000003.10:g.150395744A>G	NCBI36
NG_011800.1:g.31779T>C
NG_011800.2:g.31779T>C
NG_011800.3:g.31779T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264613.11:c.1713+3100T>C MANE Select	ENSP00000264613.6:n.1713+3100T>C
ENST00000264613.10:c.1713+3100T>C	ENSP00000264613.6:n.1713+3100T>C
ENST00000462336.5:n.87+3100T>C
ENST00000471356.1:n.532+3100T>C
ENST00000481169.5:c.1713+3100T>C	ENSP00000418773.1:n.1713+3100T>C
ENST00000489736.5:n.938+3100T>C
ENST00000490639.5:n.1745+3100T>C
ENST00000494544.1:c.1062+3100T>C	ENSP00000420545.1:n.1062+3100T>C
ENST00000497797.5:n.322+3100T>C
NM_000096.3:c.1713+3100T>C	NP_000087.1:n.1713+3100T>C
NR_046371.1:n.1966+3100T>C
XM_006713499.2:c.1713+3100T>C	XP_006713562.1:n.1713+3100T>C
XM_006713500.2:c.1713+3100T>C	XP_006713563.1:n.1713+3100T>C
XM_006713501.2:c.1713+3100T>C	XP_006713564.1:n.1713+3100T>C
XM_006713502.2:c.1713+3100T>C	XP_006713565.1:n.1713+3100T>C
XM_011512435.1:c.1713+3100T>C	XP_011510737.1:n.1713+3100T>C
XR_427361.2:n.1971+3100T>C
XM_006713499.3:c.1713+3100T>C	XP_006713562.1:n.1713+3100T>C
XM_006713500.4:c.1713+3100T>C	XP_006713563.1:n.1713+3100T>C
XM_006713501.3:c.1713+3100T>C	XP_006713564.1:n.1713+3100T>C
XM_011512435.2:c.1713+3100T>C	XP_011510737.1:n.1713+3100T>C
XM_017005734.2:c.1713+3100T>C	XP_016861223.1:n.1713+3100T>C
XM_017005735.2:c.1713+3100T>C	XP_016861224.1:n.1713+3100T>C
XR_427361.3:n.1929+3100T>C
NM_000096.4:c.1713+3100T>C MANE Select	NP_000087.2:n.1713+3100T>C
NR_046371.2:n.1750+3100T>C