Canonical Allele Identifier: CA493797209

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16248778G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154921G>A , CM000678.2:g.16154921G>A	GRCh38
NC_000016.9:g.16248778G>A , CM000678.1:g.16248778G>A	GRCh37
NC_000016.8:g.16156279G>A	NCBI36
NG_007558.2:g.73551C>T
NG_007558.3:g.73697C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000576204.6:n.856C>T
ENST00000622290.5:c.*165C>T	ENSP00000483331.2:n.*165C>T
ENST00000205557.12:c.3993C>T MANE Select	ENSP00000205557.7:p.Ala1331=
ENST00000640696.1:c.807C>T	ENSP00000492197.1:p.Ala269=
ENST00000205557.11:c.3993C>T	ENSP00000205557.7:p.Ala1331=
ENST00000456970.6:c.3618C>T	ENSP00000405002.2:n.3618C>T
ENST00000576204.5:n.856C>T
ENST00000622290.4:c.*1202C>T	ENSP00000483331.1:n.*1202C>T
NM_001171.5:c.3993C>T	NP_001162.4:p.Ala1331=
XM_011522479.1:c.3960C>T	XP_011520781.1:p.Ala1320=
XM_011522480.1:c.3651C>T	XP_011520782.1:p.Ala1217=
XM_011522481.1:c.3651C>T	XP_011520783.1:p.Ala1217=
XR_933134.1:n.539-4860G>A
NM_001351800.1:c.3651C>T	NP_001338729.1:p.Ala1217=
NR_147784.1:n.3655C>T
XM_011522479.2:c.3960C>T	XP_011520781.1:p.Ala1320=
XM_011522481.3:c.3651C>T	XP_011520783.1:p.Ala1217=
XM_017023212.1:c.3825C>T	XP_016878701.1:p.Ala1275=
XM_024450261.1:c.4029C>T	XP_024306029.1:p.Ala1343=
NM_001171.6:c.3993C>T MANE Select	NP_001162.5:p.Ala1331=