Canonical Allele Identifier: CA2806038018

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16155164_16155165insAC , CM000678.2:g.16155164_16155165insAC	GRCh38
NC_000016.9:g.16249021_16249022insAC , CM000678.1:g.16249021_16249022insAC	GRCh37
NC_000016.8:g.16156522_16156523insAC	NCBI36
NG_007558.2:g.73307_73308insGT
NG_007558.3:g.73453_73454insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.612_613insGT
ENST00000622290.5:c.*55-134_*55-133insGT	ENSP00000483331.2:n.*55-134_*55-133insGT
ENST00000205557.12:c.3883-134_3883-133insGT MANE Select	ENSP00000205557.7:n.3883-134_3883-133insGT
ENST00000640696.1:c.697-134_697-133insGT	ENSP00000492197.1:n.697-134_697-133insGT
ENST00000205557.11:c.3883-134_3883-133insGT	ENSP00000205557.7:n.3883-134_3883-133insGT
ENST00000456970.6:c.3508-134_3508-133insGT	ENSP00000405002.2:n.3508-134_3508-133insGT
ENST00000576204.5:n.612_613insGT
ENST00000622290.4:c.*1092-134_*1092-133insGT	ENSP00000483331.1:n.*1092-134_*1092-133insGT
NM_001171.5:c.3883-134_3883-133insGT	NP_001162.4:n.3883-134_3883-133insGT
XM_011522479.1:c.3850-134_3850-133insGT	XP_011520781.1:n.3850-134_3850-133insGT
XM_011522480.1:c.3541-134_3541-133insGT	XP_011520782.1:n.3541-134_3541-133insGT
XM_011522481.1:c.3541-134_3541-133insGT	XP_011520783.1:n.3541-134_3541-133insGT
XR_932836.1:n.4181-134_4181-133insGT
XR_932837.1:n.3919-134_3919-133insGT
XR_932838.1:n.3982-134_3982-133insGT
XR_933134.1:n.539-4617_539-4616insAC
NM_001351800.1:c.3541-134_3541-133insGT	NP_001338729.1:n.3541-134_3541-133insGT
NR_147784.1:n.3545-134_3545-133insGT
XM_011522479.2:c.3850-134_3850-133insGT	XP_011520781.1:n.3850-134_3850-133insGT
XM_011522481.3:c.3541-134_3541-133insGT	XP_011520783.1:n.3541-134_3541-133insGT
XM_017023212.1:c.3715-134_3715-133insGT	XP_016878701.1:n.3715-134_3715-133insGT
XM_024450261.1:c.3919-134_3919-133insGT	XP_024306029.1:n.3919-134_3919-133insGT
XR_932836.2:n.4127-134_4127-133insGT
XR_932837.3:n.3864-134_3864-133insGT
XR_932838.3:n.3927-134_3927-133insGT
NM_001171.6:c.3883-134_3883-133insGT MANE Select	NP_001162.5:n.3883-134_3883-133insGT