Canonical Allele Identifier: CA493799721

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16248628A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154771A>C , CM000678.2:g.16154771A>C	GRCh38
NC_000016.9:g.16248628A>C , CM000678.1:g.16248628A>C	GRCh37
NC_000016.8:g.16156129A>C	NCBI36
NG_007558.2:g.73701T>G
NG_007558.3:g.73847T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.928T>G
ENST00000622290.5:c.*237T>G	ENSP00000483331.2:n.*237T>G
ENST00000205557.12:c.4065T>G MANE Select	ENSP00000205557.7:p.Ser1355=
ENST00000640696.1:c.879T>G	ENSP00000492197.1:p.Ser293=
ENST00000205557.11:c.4065T>G	ENSP00000205557.7:p.Ser1355=
ENST00000456970.6:c.3690T>G	ENSP00000405002.2:n.3690T>G
ENST00000576204.5:n.928T>G
ENST00000622290.4:c.*1274T>G	ENSP00000483331.1:n.*1274T>G
NM_001171.5:c.4065T>G	NP_001162.4:p.Ser1355=
XM_011522479.1:c.4032T>G	XP_011520781.1:p.Ser1344=
XM_011522480.1:c.3723T>G	XP_011520782.1:p.Ser1241=
XM_011522481.1:c.3723T>G	XP_011520783.1:p.Ser1241=
XR_933134.1:n.539-5010A>C
NM_001351800.1:c.3723T>G	NP_001338729.1:p.Ser1241=
NR_147784.1:n.3727T>G
XM_011522479.2:c.4032T>G	XP_011520781.1:p.Ser1344=
XM_011522481.3:c.3723T>G	XP_011520783.1:p.Ser1241=
XM_017023212.1:c.3897T>G	XP_016878701.1:p.Ser1299=
XM_024450261.1:c.4101T>G	XP_024306029.1:p.Ser1367=
NM_001171.6:c.4065T>G MANE Select	NP_001162.5:p.Ser1355=