Canonical Allele Identifier: CA1410105040

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186396_149186400delinsTAGGA , CM000665.2:g.149186396_149186400delinsTAGGA	GRCh38
NC_000003.11:g.148904183_148904187delinsTAGGA , CM000665.1:g.148904183_148904187delinsTAGGA	GRCh37
NC_000003.10:g.150386873_150386877delinsTAGGA	NCBI36
NG_011800.1:g.40646_40650delinsTCCTA
NG_011800.2:g.40646_40650delinsTCCTA
NG_011800.3:g.40646_40650delinsTCCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2077+120_2077+124delinsTCCTA MANE Select	ENSP00000264613.6:n.2077+120_2077+124delinsTCCTA
ENST00000264613.10:c.2077+120_2077+124delinsTCCTA	ENSP00000264613.6:n.2077+120_2077+124delinsTCCTA
ENST00000462336.5:n.451+120_451+124delinsTCCTA
ENST00000481169.5:c.1865-954_1865-950delinsTCCTA	ENSP00000418773.1:n.1865-954_1865-950delinsTCCTA
ENST00000489736.5:n.1422_1426delinsTCCTA
ENST00000490639.5:n.2109+120_2109+124delinsTCCTA
ENST00000494544.1:c.1426+120_1426+124delinsTCCTA	ENSP00000420545.1:n.1426+120_1426+124delinsTCCTA
ENST00000497902.5:n.258+120_258+124delinsTCCTA
NM_000096.3:c.2077+120_2077+124delinsTCCTA	NP_000087.1:n.2077+120_2077+124delinsTCCTA
NR_046371.1:n.2118-954_2118-950delinsTCCTA
XM_006713499.2:c.2077+120_2077+124delinsTCCTA	XP_006713562.1:n.2077+120_2077+124delinsTCCTA
XM_006713500.2:c.2077+120_2077+124delinsTCCTA	XP_006713563.1:n.2077+120_2077+124delinsTCCTA
XM_006713501.2:c.2077+120_2077+124delinsTCCTA	XP_006713564.1:n.2077+120_2077+124delinsTCCTA
XM_006713502.2:c.2077+120_2077+124delinsTCCTA	XP_006713565.1:n.2077+120_2077+124delinsTCCTA
XM_011512435.1:c.2077+120_2077+124delinsTCCTA	XP_011510737.1:n.2077+120_2077+124delinsTCCTA
XR_427361.2:n.2335+120_2335+124delinsTCCTA
XM_006713499.3:c.2077+120_2077+124delinsTCCTA	XP_006713562.1:n.2077+120_2077+124delinsTCCTA
XM_006713500.4:c.2077+120_2077+124delinsTCCTA	XP_006713563.1:n.2077+120_2077+124delinsTCCTA
XM_006713501.3:c.2077+120_2077+124delinsTCCTA	XP_006713564.1:n.2077+120_2077+124delinsTCCTA
XM_011512435.2:c.2077+120_2077+124delinsTCCTA	XP_011510737.1:n.2077+120_2077+124delinsTCCTA
XM_017005734.2:c.2077+120_2077+124delinsTCCTA	XP_016861223.1:n.2077+120_2077+124delinsTCCTA
XM_017005735.2:c.2077+120_2077+124delinsTCCTA	XP_016861224.1:n.2077+120_2077+124delinsTCCTA
XR_427361.3:n.2293+120_2293+124delinsTCCTA
NM_000096.4:c.2077+120_2077+124delinsTCCTA MANE Select	NP_000087.2:n.2077+120_2077+124delinsTCCTA
NR_046371.2:n.1902-954_1902-950delinsTCCTA