Canonical Allele Identifier: CA1410105761

Gene: CP

Linked Data

• dbSNP Id: rs1726230935

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149187136_149187137insT , CM000665.2:g.149187136_149187137insT	GRCh38
NC_000003.11:g.148904923_148904924insT , CM000665.1:g.148904923_148904924insT	GRCh37
NC_000003.10:g.150387613_150387614insT	NCBI36
NG_011800.1:g.39909_39910insA
NG_011800.2:g.39909_39910insA
NG_011800.3:g.39909_39910insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.1865-405_1865-404insA MANE Select	ENSP00000264613.6:n.1865-405_1865-404insA
ENST00000264613.10:c.1865-405_1865-404insA	ENSP00000264613.6:n.1865-405_1865-404insA
ENST00000462336.5:n.239-405_239-404insA
ENST00000481169.5:c.1864+915_1864+916insA	ENSP00000418773.1:n.1864+915_1864+916insA
ENST00000489736.5:n.1090-405_1090-404insA
ENST00000490639.5:n.1897-405_1897-404insA
ENST00000494544.1:c.1214-405_1214-404insA	ENSP00000420545.1:n.1214-405_1214-404insA
ENST00000497902.5:n.46-405_46-404insA
NM_000096.3:c.1865-405_1865-404insA	NP_000087.1:n.1865-405_1865-404insA
NR_046371.1:n.2117+915_2117+916insA
XM_006713499.2:c.1865-405_1865-404insA	XP_006713562.1:n.1865-405_1865-404insA
XM_006713500.2:c.1865-405_1865-404insA	XP_006713563.1:n.1865-405_1865-404insA
XM_006713501.2:c.1865-405_1865-404insA	XP_006713564.1:n.1865-405_1865-404insA
XM_006713502.2:c.1865-405_1865-404insA	XP_006713565.1:n.1865-405_1865-404insA
XM_011512435.1:c.1865-405_1865-404insA	XP_011510737.1:n.1865-405_1865-404insA
XR_427361.2:n.2123-405_2123-404insA
XM_006713499.3:c.1865-405_1865-404insA	XP_006713562.1:n.1865-405_1865-404insA
XM_006713500.4:c.1865-405_1865-404insA	XP_006713563.1:n.1865-405_1865-404insA
XM_006713501.3:c.1865-405_1865-404insA	XP_006713564.1:n.1865-405_1865-404insA
XM_011512435.2:c.1865-405_1865-404insA	XP_011510737.1:n.1865-405_1865-404insA
XM_017005734.2:c.1865-405_1865-404insA	XP_016861223.1:n.1865-405_1865-404insA
XM_017005735.2:c.1865-405_1865-404insA	XP_016861224.1:n.1865-405_1865-404insA
XR_427361.3:n.2081-405_2081-404insA
NM_000096.4:c.1865-405_1865-404insA MANE Select	NP_000087.2:n.1865-405_1865-404insA
NR_046371.2:n.1901+915_1901+916insA