Canonical Allele Identifier: CA2631961080

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16149715-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16149715G>A , CM000678.2:g.16149715G>A	GRCh38
NC_000016.9:g.16243572G>A , CM000678.1:g.16243572G>A	GRCh37
NC_000016.8:g.16151073G>A	NCBI36
NG_007558.2:g.78757C>T
NG_007558.3:g.78903C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*1102C>T	ENSP00000483331.2:n.*1102C>T
ENST00000205557.12:c.*418C>T MANE Select	ENSP00000205557.7:n.*418C>T
ENST00000640696.1:c.1744C>T	ENSP00000492197.1:n.1744C>T
ENST00000205557.11:c.*418C>T	ENSP00000205557.7:n.*418C>T
ENST00000576204.5:n.1793C>T
ENST00000622290.4:c.*2139C>T	ENSP00000483331.1:n.*2139C>T
NM_001171.5:c.*418C>T	NP_001162.4:n.*418C>T
XM_011522479.1:c.*418C>T	XP_011520781.1:n.*418C>T
XM_011522480.1:c.*418C>T	XP_011520782.1:n.*418C>T
XM_011522481.1:c.*418C>T	XP_011520783.1:n.*418C>T
XR_933134.1:n.538+5425G>A
NM_001351800.1:c.*418C>T	NP_001338729.1:n.*418C>T
NR_147784.1:n.4592C>T
XM_011522479.2:c.*418C>T	XP_011520781.1:n.*418C>T
XM_011522481.3:c.*418C>T	XP_011520783.1:n.*418C>T
XM_017023212.1:c.*418C>T	XP_016878701.1:n.*418C>T
XM_024450261.1:c.*418C>T	XP_024306029.1:n.*418C>T
NM_001171.6:c.*418C>T MANE Select	NP_001162.5:n.*418C>T