Canonical Allele Identifier: CA2631963637

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16150803-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150803_16150804insC , CM000678.2:g.16150803_16150804insC	GRCh38
NC_000016.9:g.16244660_16244661insC , CM000678.1:g.16244660_16244661insC	GRCh37
NC_000016.8:g.16152161_16152162insC	NCBI36
NG_007558.2:g.77668_77669insG
NG_007558.3:g.77814_77815insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*381-32_*381-31insG	ENSP00000483331.2:n.*381-32_*381-31insG
ENST00000205557.12:c.4209-32_4209-31insG MANE Select	ENSP00000205557.7:n.4209-32_4209-31insG
ENST00000640696.1:c.1023-32_1023-31insG	ENSP00000492197.1:n.1023-32_1023-31insG
ENST00000205557.11:c.4209-32_4209-31insG	ENSP00000205557.7:n.4209-32_4209-31insG
ENST00000456970.6:c.3834-32_3834-31insG	ENSP00000405002.2:n.3834-32_3834-31insG
ENST00000576204.5:n.1072-32_1072-31insG
ENST00000622290.4:c.*1418-32_*1418-31insG	ENSP00000483331.1:n.*1418-32_*1418-31insG
NM_001171.5:c.4209-32_4209-31insG	NP_001162.4:n.4209-32_4209-31insG
XM_011522479.1:c.4176-32_4176-31insG	XP_011520781.1:n.4176-32_4176-31insG
XM_011522480.1:c.3867-32_3867-31insG	XP_011520782.1:n.3867-32_3867-31insG
XM_011522481.1:c.3867-32_3867-31insG	XP_011520783.1:n.3867-32_3867-31insG
XR_933134.1:n.538+6513_538+6514insC
NM_001351800.1:c.3867-32_3867-31insG	NP_001338729.1:n.3867-32_3867-31insG
NR_147784.1:n.3871-32_3871-31insG
XM_011522479.2:c.4176-32_4176-31insG	XP_011520781.1:n.4176-32_4176-31insG
XM_011522481.3:c.3867-32_3867-31insG	XP_011520783.1:n.3867-32_3867-31insG
XM_017023212.1:c.4041-32_4041-31insG	XP_016878701.1:n.4041-32_4041-31insG
XM_024450261.1:c.4245-32_4245-31insG	XP_024306029.1:n.4245-32_4245-31insG
NM_001171.6:c.4209-32_4209-31insG MANE Select	NP_001162.5:n.4209-32_4209-31insG