Canonical Allele Identifier: CA2806037415

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150836_16150837insA , CM000678.2:g.16150836_16150837insA	GRCh38
NC_000016.9:g.16244693_16244694insA , CM000678.1:g.16244693_16244694insA	GRCh37
NC_000016.8:g.16152194_16152195insA	NCBI36
NG_007558.2:g.77635_77636insT
NG_007558.3:g.77781_77782insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*381-65_*381-64insT	ENSP00000483331.2:n.*381-65_*381-64insT
ENST00000205557.12:c.4209-65_4209-64insT MANE Select	ENSP00000205557.7:n.4209-65_4209-64insT
ENST00000640696.1:c.1023-65_1023-64insT	ENSP00000492197.1:n.1023-65_1023-64insT
ENST00000205557.11:c.4209-65_4209-64insT	ENSP00000205557.7:n.4209-65_4209-64insT
ENST00000456970.6:c.3834-65_3834-64insT	ENSP00000405002.2:n.3834-65_3834-64insT
ENST00000576204.5:n.1072-65_1072-64insT
ENST00000622290.4:c.*1418-65_*1418-64insT	ENSP00000483331.1:n.*1418-65_*1418-64insT
NM_001171.5:c.4209-65_4209-64insT	NP_001162.4:n.4209-65_4209-64insT
XM_011522479.1:c.4176-65_4176-64insT	XP_011520781.1:n.4176-65_4176-64insT
XM_011522480.1:c.3867-65_3867-64insT	XP_011520782.1:n.3867-65_3867-64insT
XM_011522481.1:c.3867-65_3867-64insT	XP_011520783.1:n.3867-65_3867-64insT
XR_933134.1:n.538+6546_538+6547insA
NM_001351800.1:c.3867-65_3867-64insT	NP_001338729.1:n.3867-65_3867-64insT
NR_147784.1:n.3871-65_3871-64insT
XM_011522479.2:c.4176-65_4176-64insT	XP_011520781.1:n.4176-65_4176-64insT
XM_011522481.3:c.3867-65_3867-64insT	XP_011520783.1:n.3867-65_3867-64insT
XM_017023212.1:c.4041-65_4041-64insT	XP_016878701.1:n.4041-65_4041-64insT
XM_024450261.1:c.4245-65_4245-64insT	XP_024306029.1:n.4245-65_4245-64insT
NM_001171.6:c.4209-65_4209-64insT MANE Select	NP_001162.5:n.4209-65_4209-64insT