Canonical Allele Identifier: CA2661209

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149207536A>G , CM000665.2:g.149207536A>G	GRCh38
NC_000003.11:g.148925323A>G , CM000665.1:g.148925323A>G	GRCh37
NC_000003.10:g.150408013A>G	NCBI36
NG_011800.1:g.19510T>C
NG_011800.2:g.19510T>C
NG_011800.3:g.19510T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000096.4:c.863T>C MANE Select	NP_000087.2:p.Met288Thr
ENST00000264613.11:c.863T>C MANE Select	ENSP00000264613.6:p.Met288Thr
NM_000096.3:c.863T>C	NP_000087.1:p.Met288Thr
NR_046371.1:n.1116T>C
NR_046371.2:n.900T>C
ENST00000264613.10:c.863T>C	ENSP00000264613.6:p.Met288Thr
ENST00000481169.5:c.863T>C	ENSP00000418773.1:p.Met288Thr
ENST00000489736.5:n.88T>C
ENST00000490639.5:n.895T>C
ENST00000494544.1:c.212T>C	ENSP00000420545.1:p.Met71Thr
XM_006713499.2:c.863T>C	XP_006713562.1:p.Met288Thr
XM_006713499.3:c.863T>C	XP_006713562.1:p.Met288Thr
XM_006713500.2:c.863T>C	XP_006713563.1:p.Met288Thr
XM_006713500.4:c.863T>C	XP_006713563.1:p.Met288Thr
XM_006713501.2:c.863T>C	XP_006713564.1:p.Met288Thr
XM_006713501.3:c.863T>C	XP_006713564.1:p.Met288Thr
XM_006713502.2:c.863T>C	XP_006713565.1:p.Met288Thr
XM_011512435.1:c.863T>C	XP_011510737.1:p.Met288Thr
XM_011512435.2:c.863T>C	XP_011510737.1:p.Met288Thr
XM_017005734.2:c.863T>C	XP_016861223.1:p.Met288Thr
XM_017005735.2:c.863T>C	XP_016861224.1:p.Met288Thr
XR_427361.2:n.1121T>C
XR_427361.3:n.1079T>C