Canonical Allele Identifier: CA2806037432

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150873_16150874insACA , CM000678.2:g.16150873_16150874insACA	GRCh38
NC_000016.9:g.16244730_16244731insACA , CM000678.1:g.16244730_16244731insACA	GRCh37
NC_000016.8:g.16152231_16152232insACA	NCBI36
NG_007558.2:g.77598_77599insTGT
NG_007558.3:g.77744_77745insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*381-102_*381-101insTGT	ENSP00000483331.2:n.*381-102_*381-101insTGT
ENST00000205557.12:c.4209-102_4209-101insTGT MANE Select	ENSP00000205557.7:n.4209-102_4209-101insTGT
ENST00000640696.1:c.1023-102_1023-101insTGT	ENSP00000492197.1:n.1023-102_1023-101insTGT
ENST00000205557.11:c.4209-102_4209-101insTGT	ENSP00000205557.7:n.4209-102_4209-101insTGT
ENST00000456970.6:c.3834-102_3834-101insTGT	ENSP00000405002.2:n.3834-102_3834-101insTGT
ENST00000576204.5:n.1072-102_1072-101insTGT
ENST00000622290.4:c.*1418-102_*1418-101insTGT	ENSP00000483331.1:n.*1418-102_*1418-101insTGT
NM_001171.5:c.4209-102_4209-101insTGT	NP_001162.4:n.4209-102_4209-101insTGT
XM_011522479.1:c.4176-102_4176-101insTGT	XP_011520781.1:n.4176-102_4176-101insTGT
XM_011522480.1:c.3867-102_3867-101insTGT	XP_011520782.1:n.3867-102_3867-101insTGT
XM_011522481.1:c.3867-102_3867-101insTGT	XP_011520783.1:n.3867-102_3867-101insTGT
XR_933134.1:n.538+6583_538+6584insACA
NM_001351800.1:c.3867-102_3867-101insTGT	NP_001338729.1:n.3867-102_3867-101insTGT
NR_147784.1:n.3871-102_3871-101insTGT
XM_011522479.2:c.4176-102_4176-101insTGT	XP_011520781.1:n.4176-102_4176-101insTGT
XM_011522481.3:c.3867-102_3867-101insTGT	XP_011520783.1:n.3867-102_3867-101insTGT
XM_017023212.1:c.4041-102_4041-101insTGT	XP_016878701.1:n.4041-102_4041-101insTGT
XM_024450261.1:c.4245-102_4245-101insTGT	XP_024306029.1:n.4245-102_4245-101insTGT
NM_001171.6:c.4209-102_4209-101insTGT MANE Select	NP_001162.5:n.4209-102_4209-101insTGT