Canonical Allele Identifier: CA2631961352

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16149916-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16149916A>T , CM000678.2:g.16149916A>T	GRCh38
NC_000016.9:g.16243773A>T , CM000678.1:g.16243773A>T	GRCh37
NC_000016.8:g.16151274A>T	NCBI36
NG_007558.2:g.78556T>A
NG_007558.3:g.78702T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*901T>A	ENSP00000483331.2:n.*901T>A
ENST00000205557.12:c.*217T>A MANE Select	ENSP00000205557.7:n.*217T>A
ENST00000640696.1:c.1543T>A	ENSP00000492197.1:n.1543T>A
ENST00000205557.11:c.*217T>A	ENSP00000205557.7:n.*217T>A
ENST00000576204.5:n.1592T>A
ENST00000622290.4:c.*1938T>A	ENSP00000483331.1:n.*1938T>A
NM_001171.5:c.*217T>A	NP_001162.4:n.*217T>A
XM_011522479.1:c.*217T>A	XP_011520781.1:n.*217T>A
XM_011522480.1:c.*217T>A	XP_011520782.1:n.*217T>A
XM_011522481.1:c.*217T>A	XP_011520783.1:n.*217T>A
XR_933134.1:n.538+5626A>T
NM_001351800.1:c.*217T>A	NP_001338729.1:n.*217T>A
NR_147784.1:n.4391T>A
XM_011522479.2:c.*217T>A	XP_011520781.1:n.*217T>A
XM_011522481.3:c.*217T>A	XP_011520783.1:n.*217T>A
XM_017023212.1:c.*217T>A	XP_016878701.1:n.*217T>A
XM_024450261.1:c.*217T>A	XP_024306029.1:n.*217T>A
NM_001171.6:c.*217T>A MANE Select	NP_001162.5:n.*217T>A