Canonical Allele Identifier: CA2806037447

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150880_16150881insACAT , CM000678.2:g.16150880_16150881insACAT	GRCh38
NC_000016.9:g.16244737_16244738insACAT , CM000678.1:g.16244737_16244738insACAT	GRCh37
NC_000016.8:g.16152238_16152239insACAT	NCBI36
NG_007558.2:g.77591_77592insATGT
NG_007558.3:g.77737_77738insATGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*381-109_*381-108insATGT	ENSP00000483331.2:n.*381-109_*381-108insATGT
ENST00000205557.12:c.4209-109_4209-108insATGT MANE Select	ENSP00000205557.7:n.4209-109_4209-108insATGT
ENST00000640696.1:c.1023-109_1023-108insATGT	ENSP00000492197.1:n.1023-109_1023-108insATGT
ENST00000205557.11:c.4209-109_4209-108insATGT	ENSP00000205557.7:n.4209-109_4209-108insATGT
ENST00000456970.6:c.3834-109_3834-108insATGT	ENSP00000405002.2:n.3834-109_3834-108insATGT
ENST00000576204.5:n.1072-109_1072-108insATGT
ENST00000622290.4:c.*1418-109_*1418-108insATGT	ENSP00000483331.1:n.*1418-109_*1418-108insATGT
NM_001171.5:c.4209-109_4209-108insATGT	NP_001162.4:n.4209-109_4209-108insATGT
XM_011522479.1:c.4176-109_4176-108insATGT	XP_011520781.1:n.4176-109_4176-108insATGT
XM_011522480.1:c.3867-109_3867-108insATGT	XP_011520782.1:n.3867-109_3867-108insATGT
XM_011522481.1:c.3867-109_3867-108insATGT	XP_011520783.1:n.3867-109_3867-108insATGT
XR_933134.1:n.538+6590_538+6591insACAT
NM_001351800.1:c.3867-109_3867-108insATGT	NP_001338729.1:n.3867-109_3867-108insATGT
NR_147784.1:n.3871-109_3871-108insATGT
XM_011522479.2:c.4176-109_4176-108insATGT	XP_011520781.1:n.4176-109_4176-108insATGT
XM_011522481.3:c.3867-109_3867-108insATGT	XP_011520783.1:n.3867-109_3867-108insATGT
XM_017023212.1:c.4041-109_4041-108insATGT	XP_016878701.1:n.4041-109_4041-108insATGT
XM_024450261.1:c.4245-109_4245-108insATGT	XP_024306029.1:n.4245-109_4245-108insATGT
NM_001171.6:c.4209-109_4209-108insATGT MANE Select	NP_001162.5:n.4209-109_4209-108insATGT