Canonical Allele Identifier: CA2631961171

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16149811-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16149811G>T , CM000678.2:g.16149811G>T	GRCh38
NC_000016.9:g.16243668G>T , CM000678.1:g.16243668G>T	GRCh37
NC_000016.8:g.16151169G>T	NCBI36
NG_007558.2:g.78661C>A
NG_007558.3:g.78807C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*1006C>A	ENSP00000483331.2:n.*1006C>A
ENST00000205557.12:c.*322C>A MANE Select	ENSP00000205557.7:n.*322C>A
ENST00000640696.1:c.1648C>A	ENSP00000492197.1:n.1648C>A
ENST00000205557.11:c.*322C>A	ENSP00000205557.7:n.*322C>A
ENST00000576204.5:n.1697C>A
ENST00000622290.4:c.*2043C>A	ENSP00000483331.1:n.*2043C>A
NM_001171.5:c.*322C>A	NP_001162.4:n.*322C>A
XM_011522479.1:c.*322C>A	XP_011520781.1:n.*322C>A
XM_011522480.1:c.*322C>A	XP_011520782.1:n.*322C>A
XM_011522481.1:c.*322C>A	XP_011520783.1:n.*322C>A
XR_933134.1:n.538+5521G>T
NM_001351800.1:c.*322C>A	NP_001338729.1:n.*322C>A
NR_147784.1:n.4496C>A
XM_011522479.2:c.*322C>A	XP_011520781.1:n.*322C>A
XM_011522481.3:c.*322C>A	XP_011520783.1:n.*322C>A
XM_017023212.1:c.*322C>A	XP_016878701.1:n.*322C>A
XM_024450261.1:c.*322C>A	XP_024306029.1:n.*322C>A
NM_001171.6:c.*322C>A MANE Select	NP_001162.5:n.*322C>A