Canonical Allele Identifier: CA2631961161

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16149806-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16149808del , CM000678.2:g.16149808del	GRCh38
NC_000016.9:g.16243665del , CM000678.1:g.16243665del	GRCh37
NC_000016.8:g.16151166del	NCBI36
NG_007558.2:g.78665del
NG_007558.3:g.78811del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*1010del	ENSP00000483331.2:n.*1010del
ENST00000205557.12:c.*326del MANE Select	ENSP00000205557.7:n.*326del
ENST00000640696.1:c.1652del	ENSP00000492197.1:n.1652del
ENST00000205557.11:c.*326del	ENSP00000205557.7:n.*326del
ENST00000576204.5:n.1701del
ENST00000622290.4:c.*2047del	ENSP00000483331.1:n.*2047del
NM_001171.5:c.*326del	NP_001162.4:n.*326del
XM_011522479.1:c.*326del	XP_011520781.1:n.*326del
XM_011522480.1:c.*326del	XP_011520782.1:n.*326del
XM_011522481.1:c.*326del	XP_011520783.1:n.*326del
XR_933134.1:n.538+5518del
NM_001351800.1:c.*326del	NP_001338729.1:n.*326del
NR_147784.1:n.4500del
XM_011522479.2:c.*326del	XP_011520781.1:n.*326del
XM_011522481.3:c.*326del	XP_011520783.1:n.*326del
XM_017023212.1:c.*326del	XP_016878701.1:n.*326del
XM_024450261.1:c.*326del	XP_024306029.1:n.*326del
NM_001171.6:c.*326del MANE Select	NP_001162.5:n.*326del