Canonical Allele Identifier: CA2806037421

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150852_16150853insA , CM000678.2:g.16150852_16150853insA	GRCh38
NC_000016.9:g.16244709_16244710insA , CM000678.1:g.16244709_16244710insA	GRCh37
NC_000016.8:g.16152210_16152211insA	NCBI36
NG_007558.2:g.77619_77620insT
NG_007558.3:g.77765_77766insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*381-81_*381-80insT	ENSP00000483331.2:n.*381-81_*381-80insT
ENST00000205557.12:c.4209-81_4209-80insT MANE Select	ENSP00000205557.7:n.4209-81_4209-80insT
ENST00000640696.1:c.1023-81_1023-80insT	ENSP00000492197.1:n.1023-81_1023-80insT
ENST00000205557.11:c.4209-81_4209-80insT	ENSP00000205557.7:n.4209-81_4209-80insT
ENST00000456970.6:c.3834-81_3834-80insT	ENSP00000405002.2:n.3834-81_3834-80insT
ENST00000576204.5:n.1072-81_1072-80insT
ENST00000622290.4:c.*1418-81_*1418-80insT	ENSP00000483331.1:n.*1418-81_*1418-80insT
NM_001171.5:c.4209-81_4209-80insT	NP_001162.4:n.4209-81_4209-80insT
XM_011522479.1:c.4176-81_4176-80insT	XP_011520781.1:n.4176-81_4176-80insT
XM_011522480.1:c.3867-81_3867-80insT	XP_011520782.1:n.3867-81_3867-80insT
XM_011522481.1:c.3867-81_3867-80insT	XP_011520783.1:n.3867-81_3867-80insT
XR_933134.1:n.538+6562_538+6563insA
NM_001351800.1:c.3867-81_3867-80insT	NP_001338729.1:n.3867-81_3867-80insT
NR_147784.1:n.3871-81_3871-80insT
XM_011522479.2:c.4176-81_4176-80insT	XP_011520781.1:n.4176-81_4176-80insT
XM_011522481.3:c.3867-81_3867-80insT	XP_011520783.1:n.3867-81_3867-80insT
XM_017023212.1:c.4041-81_4041-80insT	XP_016878701.1:n.4041-81_4041-80insT
XM_024450261.1:c.4245-81_4245-80insT	XP_024306029.1:n.4245-81_4245-80insT
NM_001171.6:c.4209-81_4209-80insT MANE Select	NP_001162.5:n.4209-81_4209-80insT