Canonical Allele Identifier: CA2806037471

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150894_16150895insAGT , CM000678.2:g.16150894_16150895insAGT	GRCh38
NC_000016.9:g.16244751_16244752insAGT , CM000678.1:g.16244751_16244752insAGT	GRCh37
NC_000016.8:g.16152252_16152253insAGT	NCBI36
NG_007558.2:g.77577_77578insACT
NG_007558.3:g.77723_77724insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*381-123_*381-122insACT	ENSP00000483331.2:n.*381-123_*381-122insACT
ENST00000205557.12:c.4209-123_4209-122insACT MANE Select	ENSP00000205557.7:n.4209-123_4209-122insACT
ENST00000640696.1:c.1023-123_1023-122insACT	ENSP00000492197.1:n.1023-123_1023-122insACT
ENST00000205557.11:c.4209-123_4209-122insACT	ENSP00000205557.7:n.4209-123_4209-122insACT
ENST00000456970.6:c.3834-123_3834-122insACT	ENSP00000405002.2:n.3834-123_3834-122insACT
ENST00000576204.5:n.1072-123_1072-122insACT
ENST00000622290.4:c.*1418-123_*1418-122insACT	ENSP00000483331.1:n.*1418-123_*1418-122insACT
NM_001171.5:c.4209-123_4209-122insACT	NP_001162.4:n.4209-123_4209-122insACT
XM_011522479.1:c.4176-123_4176-122insACT	XP_011520781.1:n.4176-123_4176-122insACT
XM_011522480.1:c.3867-123_3867-122insACT	XP_011520782.1:n.3867-123_3867-122insACT
XM_011522481.1:c.3867-123_3867-122insACT	XP_011520783.1:n.3867-123_3867-122insACT
XR_933134.1:n.538+6604_538+6605insAGT
NM_001351800.1:c.3867-123_3867-122insACT	NP_001338729.1:n.3867-123_3867-122insACT
NR_147784.1:n.3871-123_3871-122insACT
XM_011522479.2:c.4176-123_4176-122insACT	XP_011520781.1:n.4176-123_4176-122insACT
XM_011522481.3:c.3867-123_3867-122insACT	XP_011520783.1:n.3867-123_3867-122insACT
XM_017023212.1:c.4041-123_4041-122insACT	XP_016878701.1:n.4041-123_4041-122insACT
XM_024450261.1:c.4245-123_4245-122insACT	XP_024306029.1:n.4245-123_4245-122insACT
NM_001171.6:c.4209-123_4209-122insACT MANE Select	NP_001162.5:n.4209-123_4209-122insACT