Canonical Allele Identifier: CA2806037467

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150890_16150891insGG , CM000678.2:g.16150890_16150891insGG	GRCh38
NC_000016.9:g.16244747_16244748insGG , CM000678.1:g.16244747_16244748insGG	GRCh37
NC_000016.8:g.16152248_16152249insGG	NCBI36
NG_007558.2:g.77581_77582insCC
NG_007558.3:g.77727_77728insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*381-119_*381-118insCC	ENSP00000483331.2:n.*381-119_*381-118insCC
ENST00000205557.12:c.4209-119_4209-118insCC MANE Select	ENSP00000205557.7:n.4209-119_4209-118insCC
ENST00000640696.1:c.1023-119_1023-118insCC	ENSP00000492197.1:n.1023-119_1023-118insCC
ENST00000205557.11:c.4209-119_4209-118insCC	ENSP00000205557.7:n.4209-119_4209-118insCC
ENST00000456970.6:c.3834-119_3834-118insCC	ENSP00000405002.2:n.3834-119_3834-118insCC
ENST00000576204.5:n.1072-119_1072-118insCC
ENST00000622290.4:c.*1418-119_*1418-118insCC	ENSP00000483331.1:n.*1418-119_*1418-118insCC
NM_001171.5:c.4209-119_4209-118insCC	NP_001162.4:n.4209-119_4209-118insCC
XM_011522479.1:c.4176-119_4176-118insCC	XP_011520781.1:n.4176-119_4176-118insCC
XM_011522480.1:c.3867-119_3867-118insCC	XP_011520782.1:n.3867-119_3867-118insCC
XM_011522481.1:c.3867-119_3867-118insCC	XP_011520783.1:n.3867-119_3867-118insCC
XR_933134.1:n.538+6600_538+6601insGG
NM_001351800.1:c.3867-119_3867-118insCC	NP_001338729.1:n.3867-119_3867-118insCC
NR_147784.1:n.3871-119_3871-118insCC
XM_011522479.2:c.4176-119_4176-118insCC	XP_011520781.1:n.4176-119_4176-118insCC
XM_011522481.3:c.3867-119_3867-118insCC	XP_011520783.1:n.3867-119_3867-118insCC
XM_017023212.1:c.4041-119_4041-118insCC	XP_016878701.1:n.4041-119_4041-118insCC
XM_024450261.1:c.4245-119_4245-118insCC	XP_024306029.1:n.4245-119_4245-118insCC
NM_001171.6:c.4209-119_4209-118insCC MANE Select	NP_001162.5:n.4209-119_4209-118insCC