Canonical Allele Identifier: CA1410108438

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149178614_149178618delinsTAATC , CM000665.2:g.149178614_149178618delinsTAATC	GRCh38
NC_000003.11:g.148896401_148896405delinsTAATC , CM000665.1:g.148896401_148896405delinsTAATC	GRCh37
NC_000003.10:g.150379091_150379095delinsTAATC	NCBI36
NG_011800.1:g.48428_48432delinsGATTA
NG_011800.2:g.48428_48432delinsGATTA
NG_011800.3:g.48428_48432delinsGATTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2675_2679delinsGATTA MANE Select	ENSP00000264613.6:p.Gly892=
ENST00000264613.10:c.2675_2679delinsGATTA	ENSP00000264613.6:p.Gly892=
ENST00000460674.5:n.592_596delinsGATTA
ENST00000463556.5:n.197_201delinsGATTA
ENST00000479771.5:c.80_84delinsGATTA	ENSP00000420367.1:p.Gly27=
ENST00000481169.5:c.2462_2466delinsGATTA	ENSP00000418773.1:p.Gly821=
ENST00000490639.5:n.2707_2711delinsGATTA
ENST00000494544.1:c.2024_2028delinsGATTA	ENSP00000420545.1:p.Gly675=
NM_000096.3:c.2675_2679delinsGATTA	NP_000087.1:p.Gly892=
NR_046371.1:n.2715_2719delinsGATTA
XM_006713499.2:c.2675_2679delinsGATTA	XP_006713562.1:p.Gly892=
XM_006713500.2:c.2675_2679delinsGATTA	XP_006713563.1:p.Gly892=
XM_006713501.2:c.2675_2679delinsGATTA	XP_006713564.1:p.Gly892=
XM_011512435.1:c.2675_2679delinsGATTA	XP_011510737.1:p.Gly892=
XR_427361.2:n.2933_2937delinsGATTA
XM_006713499.3:c.2675_2679delinsGATTA	XP_006713562.1:p.Gly892=
XM_006713500.4:c.2675_2679delinsGATTA	XP_006713563.1:p.Gly892=
XM_006713501.3:c.2675_2679delinsGATTA	XP_006713564.1:p.Gly892=
XM_011512435.2:c.2675_2679delinsGATTA	XP_011510737.1:p.Gly892=
XM_017005734.2:c.2675_2679delinsGATTA	XP_016861223.1:p.Gly892=
XM_017005735.2:c.2675_2679delinsGATTA	XP_016861224.1:p.Gly892=
XR_427361.3:n.2891_2895delinsGATTA
NM_000096.4:c.2675_2679delinsGATTA MANE Select	NP_000087.2:p.Gly892=
NR_046371.2:n.2499_2503delinsGATTA