Canonical Allele Identifier: CA2806038005

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16155150_16155151insACA , CM000678.2:g.16155150_16155151insACA	GRCh38
NC_000016.9:g.16249007_16249008insACA , CM000678.1:g.16249007_16249008insACA	GRCh37
NC_000016.8:g.16156508_16156509insACA	NCBI36
NG_007558.2:g.73321_73322insTGT
NG_007558.3:g.73467_73468insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.626_627insTGT
ENST00000622290.5:c.*55-120_*55-119insTGT	ENSP00000483331.2:n.*55-120_*55-119insTGT
ENST00000205557.12:c.3883-120_3883-119insTGT MANE Select	ENSP00000205557.7:n.3883-120_3883-119insTGT
ENST00000640696.1:c.697-120_697-119insTGT	ENSP00000492197.1:n.697-120_697-119insTGT
ENST00000205557.11:c.3883-120_3883-119insTGT	ENSP00000205557.7:n.3883-120_3883-119insTGT
ENST00000456970.6:c.3508-120_3508-119insTGT	ENSP00000405002.2:n.3508-120_3508-119insTGT
ENST00000576204.5:n.626_627insTGT
ENST00000622290.4:c.*1092-120_*1092-119insTGT	ENSP00000483331.1:n.*1092-120_*1092-119insTGT
NM_001171.5:c.3883-120_3883-119insTGT	NP_001162.4:n.3883-120_3883-119insTGT
XM_011522479.1:c.3850-120_3850-119insTGT	XP_011520781.1:n.3850-120_3850-119insTGT
XM_011522480.1:c.3541-120_3541-119insTGT	XP_011520782.1:n.3541-120_3541-119insTGT
XM_011522481.1:c.3541-120_3541-119insTGT	XP_011520783.1:n.3541-120_3541-119insTGT
XR_932836.1:n.4181-120_4181-119insTGT
XR_932837.1:n.3919-120_3919-119insTGT
XR_932838.1:n.3982-120_3982-119insTGT
XR_933134.1:n.539-4631_539-4630insACA
NM_001351800.1:c.3541-120_3541-119insTGT	NP_001338729.1:n.3541-120_3541-119insTGT
NR_147784.1:n.3545-120_3545-119insTGT
XM_011522479.2:c.3850-120_3850-119insTGT	XP_011520781.1:n.3850-120_3850-119insTGT
XM_011522481.3:c.3541-120_3541-119insTGT	XP_011520783.1:n.3541-120_3541-119insTGT
XM_017023212.1:c.3715-120_3715-119insTGT	XP_016878701.1:n.3715-120_3715-119insTGT
XM_024450261.1:c.3919-120_3919-119insTGT	XP_024306029.1:n.3919-120_3919-119insTGT
XR_932836.2:n.4127-120_4127-119insTGT
XR_932837.3:n.3864-120_3864-119insTGT
XR_932838.3:n.3927-120_3927-119insTGT
NM_001171.6:c.3883-120_3883-119insTGT MANE Select	NP_001162.5:n.3883-120_3883-119insTGT