Canonical Allele Identifier: CA2806038133

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16155235_16155236insACAG , CM000678.2:g.16155235_16155236insACAG	GRCh38
NC_000016.9:g.16249092_16249093insACAG , CM000678.1:g.16249092_16249093insACAG	GRCh37
NC_000016.8:g.16156593_16156594insACAG	NCBI36
NG_007558.2:g.73236_73237insCTGT
NG_007558.3:g.73382_73383insCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.541_542insCTGT
ENST00000622290.5:c.*55-205_*55-204insCTGT	ENSP00000483331.2:n.*55-205_*55-204insCTGT
ENST00000205557.12:c.3883-205_3883-204insCTGT MANE Select	ENSP00000205557.7:n.3883-205_3883-204insCTGT
ENST00000640696.1:c.697-205_697-204insCTGT	ENSP00000492197.1:n.697-205_697-204insCTGT
ENST00000205557.11:c.3883-205_3883-204insCTGT	ENSP00000205557.7:n.3883-205_3883-204insCTGT
ENST00000456970.6:c.3508-205_3508-204insCTGT	ENSP00000405002.2:n.3508-205_3508-204insCTGT
ENST00000576204.5:n.541_542insCTGT
ENST00000622290.4:c.*1092-205_*1092-204insCTGT	ENSP00000483331.1:n.*1092-205_*1092-204insCTGT
NM_001171.5:c.3883-205_3883-204insCTGT	NP_001162.4:n.3883-205_3883-204insCTGT
XM_011522479.1:c.3850-205_3850-204insCTGT	XP_011520781.1:n.3850-205_3850-204insCTGT
XM_011522480.1:c.3541-205_3541-204insCTGT	XP_011520782.1:n.3541-205_3541-204insCTGT
XM_011522481.1:c.3541-205_3541-204insCTGT	XP_011520783.1:n.3541-205_3541-204insCTGT
XR_932836.1:n.4181-205_4181-204insCTGT
XR_932837.1:n.3919-205_3919-204insCTGT
XR_932838.1:n.3982-205_3982-204insCTGT
XR_933134.1:n.539-4546_539-4545insACAG
NM_001351800.1:c.3541-205_3541-204insCTGT	NP_001338729.1:n.3541-205_3541-204insCTGT
NR_147784.1:n.3545-205_3545-204insCTGT
XM_011522479.2:c.3850-205_3850-204insCTGT	XP_011520781.1:n.3850-205_3850-204insCTGT
XM_011522481.3:c.3541-205_3541-204insCTGT	XP_011520783.1:n.3541-205_3541-204insCTGT
XM_017023212.1:c.3715-205_3715-204insCTGT	XP_016878701.1:n.3715-205_3715-204insCTGT
XM_024450261.1:c.3919-205_3919-204insCTGT	XP_024306029.1:n.3919-205_3919-204insCTGT
XR_932836.2:n.4127-205_4127-204insCTGT
XR_932837.3:n.3864-205_3864-204insCTGT
XR_932838.3:n.3927-205_3927-204insCTGT
NM_001171.6:c.3883-205_3883-204insCTGT MANE Select	NP_001162.5:n.3883-205_3883-204insCTGT