Canonical Allele Identifier: CA493797254

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16154939-G-T
• MyVariant Identifiers: chr16:g.16248796G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154939G>T , CM000678.2:g.16154939G>T	GRCh38
NC_000016.9:g.16248796G>T , CM000678.1:g.16248796G>T	GRCh37
NC_000016.8:g.16156297G>T	NCBI36
NG_007558.2:g.73533C>A
NG_007558.3:g.73679C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.838C>A
ENST00000622290.5:c.*147C>A	ENSP00000483331.2:n.*147C>A
ENST00000205557.12:c.3975C>A MANE Select	ENSP00000205557.7:p.Ile1325=
ENST00000640696.1:c.789C>A	ENSP00000492197.1:p.Ile263=
ENST00000205557.11:c.3975C>A	ENSP00000205557.7:p.Ile1325=
ENST00000456970.6:c.3600C>A	ENSP00000405002.2:n.3600C>A
ENST00000576204.5:n.838C>A
ENST00000622290.4:c.*1184C>A	ENSP00000483331.1:n.*1184C>A
NM_001171.5:c.3975C>A	NP_001162.4:p.Ile1325=
XM_011522479.1:c.3942C>A	XP_011520781.1:p.Ile1314=
XM_011522480.1:c.3633C>A	XP_011520782.1:p.Ile1211=
XM_011522481.1:c.3633C>A	XP_011520783.1:p.Ile1211=
XR_933134.1:n.539-4842G>T
NM_001351800.1:c.3633C>A	NP_001338729.1:p.Ile1211=
NR_147784.1:n.3637C>A
XM_011522479.2:c.3942C>A	XP_011520781.1:p.Ile1314=
XM_011522481.3:c.3633C>A	XP_011520783.1:p.Ile1211=
XM_017023212.1:c.3807C>A	XP_016878701.1:p.Ile1269=
XM_024450261.1:c.4011C>A	XP_024306029.1:p.Ile1337=
NM_001171.6:c.3975C>A MANE Select	NP_001162.5:p.Ile1325=