Canonical Allele Identifier: CA2631961447

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16149971-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16149972del , CM000678.2:g.16149972del	GRCh38
NC_000016.9:g.16243829del , CM000678.1:g.16243829del	GRCh37
NC_000016.8:g.16151330del	NCBI36
NG_007558.2:g.78500del
NG_007558.3:g.78646del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*845del	ENSP00000483331.2:n.*845del
ENST00000205557.12:c.*161del MANE Select	ENSP00000205557.7:n.*161del
ENST00000640696.1:c.1487del	ENSP00000492197.1:n.1487del
ENST00000205557.11:c.*161del	ENSP00000205557.7:n.*161del
ENST00000576204.5:n.1536del
ENST00000622290.4:c.*1882del	ENSP00000483331.1:n.*1882del
NM_001171.5:c.*161del	NP_001162.4:n.*161del
XM_011522479.1:c.*161del	XP_011520781.1:n.*161del
XM_011522480.1:c.*161del	XP_011520782.1:n.*161del
XM_011522481.1:c.*161del	XP_011520783.1:n.*161del
XR_933134.1:n.538+5682del
NM_001351800.1:c.*161del	NP_001338729.1:n.*161del
NR_147784.1:n.4335del
XM_011522479.2:c.*161del	XP_011520781.1:n.*161del
XM_011522481.3:c.*161del	XP_011520783.1:n.*161del
XM_017023212.1:c.*161del	XP_016878701.1:n.*161del
XM_024450261.1:c.*161del	XP_024306029.1:n.*161del
NM_001171.6:c.*161del MANE Select	NP_001162.5:n.*161del