Canonical Allele Identifier: CA2806037460

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150887_16150888insA , CM000678.2:g.16150887_16150888insA	GRCh38
NC_000016.9:g.16244744_16244745insA , CM000678.1:g.16244744_16244745insA	GRCh37
NC_000016.8:g.16152245_16152246insA	NCBI36
NG_007558.2:g.77584_77585insT
NG_007558.3:g.77730_77731insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*381-116_*381-115insT	ENSP00000483331.2:n.*381-116_*381-115insT
ENST00000205557.12:c.4209-116_4209-115insT MANE Select	ENSP00000205557.7:n.4209-116_4209-115insT
ENST00000640696.1:c.1023-116_1023-115insT	ENSP00000492197.1:n.1023-116_1023-115insT
ENST00000205557.11:c.4209-116_4209-115insT	ENSP00000205557.7:n.4209-116_4209-115insT
ENST00000456970.6:c.3834-116_3834-115insT	ENSP00000405002.2:n.3834-116_3834-115insT
ENST00000576204.5:n.1072-116_1072-115insT
ENST00000622290.4:c.*1418-116_*1418-115insT	ENSP00000483331.1:n.*1418-116_*1418-115insT
NM_001171.5:c.4209-116_4209-115insT	NP_001162.4:n.4209-116_4209-115insT
XM_011522479.1:c.4176-116_4176-115insT	XP_011520781.1:n.4176-116_4176-115insT
XM_011522480.1:c.3867-116_3867-115insT	XP_011520782.1:n.3867-116_3867-115insT
XM_011522481.1:c.3867-116_3867-115insT	XP_011520783.1:n.3867-116_3867-115insT
XR_933134.1:n.538+6597_538+6598insA
NM_001351800.1:c.3867-116_3867-115insT	NP_001338729.1:n.3867-116_3867-115insT
NR_147784.1:n.3871-116_3871-115insT
XM_011522479.2:c.4176-116_4176-115insT	XP_011520781.1:n.4176-116_4176-115insT
XM_011522481.3:c.3867-116_3867-115insT	XP_011520783.1:n.3867-116_3867-115insT
XM_017023212.1:c.4041-116_4041-115insT	XP_016878701.1:n.4041-116_4041-115insT
XM_024450261.1:c.4245-116_4245-115insT	XP_024306029.1:n.4245-116_4245-115insT
NM_001171.6:c.4209-116_4209-115insT MANE Select	NP_001162.5:n.4209-116_4209-115insT