Canonical Allele Identifier: CA2806037491

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150917_16150918insACA , CM000678.2:g.16150917_16150918insACA	GRCh38
NC_000016.9:g.16244774_16244775insACA , CM000678.1:g.16244774_16244775insACA	GRCh37
NC_000016.8:g.16152275_16152276insACA	NCBI36
NG_007558.2:g.77554_77555insTGT
NG_007558.3:g.77700_77701insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*381-146_*381-145insTGT	ENSP00000483331.2:n.*381-146_*381-145insTGT
ENST00000205557.12:c.4209-146_4209-145insTGT MANE Select	ENSP00000205557.7:n.4209-146_4209-145insTGT
ENST00000640696.1:c.1023-146_1023-145insTGT	ENSP00000492197.1:n.1023-146_1023-145insTGT
ENST00000205557.11:c.4209-146_4209-145insTGT	ENSP00000205557.7:n.4209-146_4209-145insTGT
ENST00000456970.6:c.3834-146_3834-145insTGT	ENSP00000405002.2:n.3834-146_3834-145insTGT
ENST00000576204.5:n.1072-146_1072-145insTGT
ENST00000622290.4:c.*1418-146_*1418-145insTGT	ENSP00000483331.1:n.*1418-146_*1418-145insTGT
NM_001171.5:c.4209-146_4209-145insTGT	NP_001162.4:n.4209-146_4209-145insTGT
XM_011522479.1:c.4176-146_4176-145insTGT	XP_011520781.1:n.4176-146_4176-145insTGT
XM_011522480.1:c.3867-146_3867-145insTGT	XP_011520782.1:n.3867-146_3867-145insTGT
XM_011522481.1:c.3867-146_3867-145insTGT	XP_011520783.1:n.3867-146_3867-145insTGT
XR_933134.1:n.538+6627_538+6628insACA
NM_001351800.1:c.3867-146_3867-145insTGT	NP_001338729.1:n.3867-146_3867-145insTGT
NR_147784.1:n.3871-146_3871-145insTGT
XM_011522479.2:c.4176-146_4176-145insTGT	XP_011520781.1:n.4176-146_4176-145insTGT
XM_011522481.3:c.3867-146_3867-145insTGT	XP_011520783.1:n.3867-146_3867-145insTGT
XM_017023212.1:c.4041-146_4041-145insTGT	XP_016878701.1:n.4041-146_4041-145insTGT
XM_024450261.1:c.4245-146_4245-145insTGT	XP_024306029.1:n.4245-146_4245-145insTGT
NM_001171.6:c.4209-146_4209-145insTGT MANE Select	NP_001162.5:n.4209-146_4209-145insTGT