Canonical Allele Identifier: CA2806037114

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159674_16159675insAA , CM000678.2:g.16159674_16159675insAA	GRCh38
NC_000016.9:g.16253531_16253532insAA , CM000678.1:g.16253531_16253532insAA	GRCh37
NC_000016.8:g.16161032_16161033insAA	NCBI36
NG_007558.2:g.68797_68798insTT
NG_007558.3:g.68943_68944insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3634-92_3634-91insTT	ENSP00000483331.2:n.3634-92_3634-91insTT
ENST00000205557.12:c.3634-92_3634-91insTT MANE Select	ENSP00000205557.7:n.3634-92_3634-91insTT
ENST00000640696.1:c.448-92_448-91insTT	ENSP00000492197.1:n.448-92_448-91insTT
ENST00000205557.11:c.3634-92_3634-91insTT	ENSP00000205557.7:n.3634-92_3634-91insTT
ENST00000456970.6:c.3259-92_3259-91insTT	ENSP00000405002.2:n.3259-92_3259-91insTT
ENST00000622290.4:c.*843-92_*843-91insTT	ENSP00000483331.1:n.*843-92_*843-91insTT
NM_001171.5:c.3634-92_3634-91insTT	NP_001162.4:n.3634-92_3634-91insTT
XM_011522479.1:c.3601-92_3601-91insTT	XP_011520781.1:n.3601-92_3601-91insTT
XM_011522480.1:c.3292-92_3292-91insTT	XP_011520782.1:n.3292-92_3292-91insTT
XM_011522481.1:c.3292-92_3292-91insTT	XP_011520783.1:n.3292-92_3292-91insTT
XR_932836.1:n.3869-92_3869-91insTT
XR_932837.1:n.3670-92_3670-91insTT
XR_932838.1:n.3670-92_3670-91insTT
XR_933133.1:n.85_86insAA
XR_933134.1:n.539-107_539-106insAA
NM_001351800.1:c.3292-92_3292-91insTT	NP_001338729.1:n.3292-92_3292-91insTT
NR_147784.1:n.3296-92_3296-91insTT
XM_011522479.2:c.3601-92_3601-91insTT	XP_011520781.1:n.3601-92_3601-91insTT
XM_011522481.3:c.3292-92_3292-91insTT	XP_011520783.1:n.3292-92_3292-91insTT
XM_017023212.1:c.3466-92_3466-91insTT	XP_016878701.1:n.3466-92_3466-91insTT
XM_024450261.1:c.3670-92_3670-91insTT	XP_024306029.1:n.3670-92_3670-91insTT
XR_932836.2:n.3815-92_3815-91insTT
XR_932837.3:n.3615-92_3615-91insTT
XR_932838.3:n.3615-92_3615-91insTT
NM_001171.6:c.3634-92_3634-91insTT MANE Select	NP_001162.5:n.3634-92_3634-91insTT