Canonical Allele Identifier: CA2210141290

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16155228_16155232delinsCTCTA , CM000678.2:g.16155228_16155232delinsCTCTA	GRCh38
NC_000016.9:g.16249085_16249089delinsCTCTA , CM000678.1:g.16249085_16249089delinsCTCTA	GRCh37
NC_000016.8:g.16156586_16156590delinsCTCTA	NCBI36
NG_007558.2:g.73240_73244delinsTAGAG
NG_007558.3:g.73386_73390delinsTAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.545_549delinsTAGAG
ENST00000622290.5:c.*55-201_*55-197delinsTAGAG	ENSP00000483331.2:n.*55-201_*55-197delinsTAGAG
ENST00000205557.12:c.3883-201_3883-197delinsTAGAG MANE Select	ENSP00000205557.7:n.3883-201_3883-197delinsTAGAG
ENST00000640696.1:c.697-201_697-197delinsTAGAG	ENSP00000492197.1:n.697-201_697-197delinsTAGAG
ENST00000205557.11:c.3883-201_3883-197delinsTAGAG	ENSP00000205557.7:n.3883-201_3883-197delinsTAGAG
ENST00000456970.6:c.3508-201_3508-197delinsTAGAG	ENSP00000405002.2:n.3508-201_3508-197delinsTAGAG
ENST00000576204.5:n.545_549delinsTAGAG
ENST00000622290.4:c.*1092-201_*1092-197delinsTAGAG	ENSP00000483331.1:n.*1092-201_*1092-197delinsTAGAG
NM_001171.5:c.3883-201_3883-197delinsTAGAG	NP_001162.4:n.3883-201_3883-197delinsTAGAG
XM_011522479.1:c.3850-201_3850-197delinsTAGAG	XP_011520781.1:n.3850-201_3850-197delinsTAGAG
XM_011522480.1:c.3541-201_3541-197delinsTAGAG	XP_011520782.1:n.3541-201_3541-197delinsTAGAG
XM_011522481.1:c.3541-201_3541-197delinsTAGAG	XP_011520783.1:n.3541-201_3541-197delinsTAGAG
XR_932836.1:n.4181-201_4181-197delinsTAGAG
XR_932837.1:n.3919-201_3919-197delinsTAGAG
XR_932838.1:n.3982-201_3982-197delinsTAGAG
XR_933134.1:n.539-4553_539-4549delinsCTCTA
NM_001351800.1:c.3541-201_3541-197delinsTAGAG	NP_001338729.1:n.3541-201_3541-197delinsTAGAG
NR_147784.1:n.3545-201_3545-197delinsTAGAG
XM_011522479.2:c.3850-201_3850-197delinsTAGAG	XP_011520781.1:n.3850-201_3850-197delinsTAGAG
XM_011522481.3:c.3541-201_3541-197delinsTAGAG	XP_011520783.1:n.3541-201_3541-197delinsTAGAG
XM_017023212.1:c.3715-201_3715-197delinsTAGAG	XP_016878701.1:n.3715-201_3715-197delinsTAGAG
XM_024450261.1:c.3919-201_3919-197delinsTAGAG	XP_024306029.1:n.3919-201_3919-197delinsTAGAG
XR_932836.2:n.4127-201_4127-197delinsTAGAG
XR_932837.3:n.3864-201_3864-197delinsTAGAG
XR_932838.3:n.3927-201_3927-197delinsTAGAG
NM_001171.6:c.3883-201_3883-197delinsTAGAG MANE Select	NP_001162.5:n.3883-201_3883-197delinsTAGAG