Canonical Allele Identifier: CA2806037477

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150904_16150905insA , CM000678.2:g.16150904_16150905insA	GRCh38
NC_000016.9:g.16244761_16244762insA , CM000678.1:g.16244761_16244762insA	GRCh37
NC_000016.8:g.16152262_16152263insA	NCBI36
NG_007558.2:g.77567_77568insT
NG_007558.3:g.77713_77714insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*381-133_*381-132insT	ENSP00000483331.2:n.*381-133_*381-132insT
ENST00000205557.12:c.4209-133_4209-132insT MANE Select	ENSP00000205557.7:n.4209-133_4209-132insT
ENST00000640696.1:c.1023-133_1023-132insT	ENSP00000492197.1:n.1023-133_1023-132insT
ENST00000205557.11:c.4209-133_4209-132insT	ENSP00000205557.7:n.4209-133_4209-132insT
ENST00000456970.6:c.3834-133_3834-132insT	ENSP00000405002.2:n.3834-133_3834-132insT
ENST00000576204.5:n.1072-133_1072-132insT
ENST00000622290.4:c.*1418-133_*1418-132insT	ENSP00000483331.1:n.*1418-133_*1418-132insT
NM_001171.5:c.4209-133_4209-132insT	NP_001162.4:n.4209-133_4209-132insT
XM_011522479.1:c.4176-133_4176-132insT	XP_011520781.1:n.4176-133_4176-132insT
XM_011522480.1:c.3867-133_3867-132insT	XP_011520782.1:n.3867-133_3867-132insT
XM_011522481.1:c.3867-133_3867-132insT	XP_011520783.1:n.3867-133_3867-132insT
XR_933134.1:n.538+6614_538+6615insA
NM_001351800.1:c.3867-133_3867-132insT	NP_001338729.1:n.3867-133_3867-132insT
NR_147784.1:n.3871-133_3871-132insT
XM_011522479.2:c.4176-133_4176-132insT	XP_011520781.1:n.4176-133_4176-132insT
XM_011522481.3:c.3867-133_3867-132insT	XP_011520783.1:n.3867-133_3867-132insT
XM_017023212.1:c.4041-133_4041-132insT	XP_016878701.1:n.4041-133_4041-132insT
XM_024450261.1:c.4245-133_4245-132insT	XP_024306029.1:n.4245-133_4245-132insT
NM_001171.6:c.4209-133_4209-132insT MANE Select	NP_001162.5:n.4209-133_4209-132insT