Canonical Allele Identifier: CA2210133355

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16149730_16149731delinsAT , CM000678.2:g.16149730_16149731delinsAT	GRCh38
NC_000016.9:g.16243587_16243588delinsAT , CM000678.1:g.16243587_16243588delinsAT	GRCh37
NC_000016.8:g.16151088_16151089delinsAT	NCBI36
NG_007558.2:g.78741_78742delinsAT
NG_007558.3:g.78887_78888delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*1086_*1087delinsAT	ENSP00000483331.2:n.*1086_*1087delinsAT
ENST00000205557.12:c.*402_*403delinsAT MANE Select	ENSP00000205557.7:n.*402_*403delinsAT
ENST00000640696.1:c.1728_1729delinsAT	ENSP00000492197.1:n.1728_1729delinsAT
ENST00000205557.11:c.*402_*403delinsAT	ENSP00000205557.7:n.*402_*403delinsAT
ENST00000576204.5:n.1777_1778delinsAT
ENST00000622290.4:c.*2123_*2124delinsAT	ENSP00000483331.1:n.*2123_*2124delinsAT
NM_001171.5:c.*402_*403delinsAT	NP_001162.4:n.*402_*403delinsAT
XM_011522479.1:c.*402_*403delinsAT	XP_011520781.1:n.*402_*403delinsAT
XM_011522480.1:c.*402_*403delinsAT	XP_011520782.1:n.*402_*403delinsAT
XM_011522481.1:c.*402_*403delinsAT	XP_011520783.1:n.*402_*403delinsAT
XR_933134.1:n.538+5440_538+5441delinsAT
NM_001351800.1:c.*402_*403delinsAT	NP_001338729.1:n.*402_*403delinsAT
NR_147784.1:n.4576_4577delinsAT
XM_011522479.2:c.*402_*403delinsAT	XP_011520781.1:n.*402_*403delinsAT
XM_011522481.3:c.*402_*403delinsAT	XP_011520783.1:n.*402_*403delinsAT
XM_017023212.1:c.*402_*403delinsAT	XP_016878701.1:n.*402_*403delinsAT
XM_024450261.1:c.*402_*403delinsAT	XP_024306029.1:n.*402_*403delinsAT
NM_001171.6:c.*402_*403delinsAT MANE Select	NP_001162.5:n.*402_*403delinsAT