Canonical Allele Identifier: CA2806037444

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150878_16150879insAGA , CM000678.2:g.16150878_16150879insAGA	GRCh38
NC_000016.9:g.16244735_16244736insAGA , CM000678.1:g.16244735_16244736insAGA	GRCh37
NC_000016.8:g.16152236_16152237insAGA	NCBI36
NG_007558.2:g.77593_77594insTCT
NG_007558.3:g.77739_77740insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*381-107_*381-106insTCT	ENSP00000483331.2:n.*381-107_*381-106insTCT
ENST00000205557.12:c.4209-107_4209-106insTCT MANE Select	ENSP00000205557.7:n.4209-107_4209-106insTCT
ENST00000640696.1:c.1023-107_1023-106insTCT	ENSP00000492197.1:n.1023-107_1023-106insTCT
ENST00000205557.11:c.4209-107_4209-106insTCT	ENSP00000205557.7:n.4209-107_4209-106insTCT
ENST00000456970.6:c.3834-107_3834-106insTCT	ENSP00000405002.2:n.3834-107_3834-106insTCT
ENST00000576204.5:n.1072-107_1072-106insTCT
ENST00000622290.4:c.*1418-107_*1418-106insTCT	ENSP00000483331.1:n.*1418-107_*1418-106insTCT
NM_001171.5:c.4209-107_4209-106insTCT	NP_001162.4:n.4209-107_4209-106insTCT
XM_011522479.1:c.4176-107_4176-106insTCT	XP_011520781.1:n.4176-107_4176-106insTCT
XM_011522480.1:c.3867-107_3867-106insTCT	XP_011520782.1:n.3867-107_3867-106insTCT
XM_011522481.1:c.3867-107_3867-106insTCT	XP_011520783.1:n.3867-107_3867-106insTCT
XR_933134.1:n.538+6588_538+6589insAGA
NM_001351800.1:c.3867-107_3867-106insTCT	NP_001338729.1:n.3867-107_3867-106insTCT
NR_147784.1:n.3871-107_3871-106insTCT
XM_011522479.2:c.4176-107_4176-106insTCT	XP_011520781.1:n.4176-107_4176-106insTCT
XM_011522481.3:c.3867-107_3867-106insTCT	XP_011520783.1:n.3867-107_3867-106insTCT
XM_017023212.1:c.4041-107_4041-106insTCT	XP_016878701.1:n.4041-107_4041-106insTCT
XM_024450261.1:c.4245-107_4245-106insTCT	XP_024306029.1:n.4245-107_4245-106insTCT
NM_001171.6:c.4209-107_4209-106insTCT MANE Select	NP_001162.5:n.4209-107_4209-106insTCT