Canonical Allele Identifier: CA394884004

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16244595C>G (hg19) ; chr16:g.16150738C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150738C>G , CM000678.2:g.16150738C>G	GRCh38
NC_000016.9:g.16244595C>G , CM000678.1:g.16244595C>G	GRCh37
NC_000016.8:g.16152096C>G	NCBI36
NG_007558.2:g.77734G>C
NG_007558.3:g.77880G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*415G>C	ENSP00000483331.2:n.*415G>C
ENST00000205557.12:c.4243G>C MANE Select	ENSP00000205557.7:p.Ala1415Pro
ENST00000640696.1:c.1057G>C	ENSP00000492197.1:p.Ala353Pro
ENST00000205557.11:c.4243G>C	ENSP00000205557.7:p.Ala1415Pro
ENST00000456970.6:c.3868G>C	ENSP00000405002.2:n.3868G>C
ENST00000576204.5:n.1106G>C
ENST00000622290.4:c.*1452G>C	ENSP00000483331.1:n.*1452G>C
NM_001171.5:c.4243G>C	NP_001162.4:p.Ala1415Pro
XM_011522479.1:c.4210G>C	XP_011520781.1:p.Ala1404Pro
XM_011522480.1:c.3901G>C	XP_011520782.1:p.Ala1301Pro
XM_011522481.1:c.3901G>C	XP_011520783.1:p.Ala1301Pro
XR_933134.1:n.538+6448C>G
NM_001351800.1:c.3901G>C	NP_001338729.1:p.Ala1301Pro
NR_147784.1:n.3905G>C
XM_011522479.2:c.4210G>C	XP_011520781.1:p.Ala1404Pro
XM_011522481.3:c.3901G>C	XP_011520783.1:p.Ala1301Pro
XM_017023212.1:c.4075G>C	XP_016878701.1:p.Ala1359Pro
XM_024450261.1:c.4279G>C	XP_024306029.1:p.Ala1427Pro
NM_001171.6:c.4243G>C MANE Select	NP_001162.5:p.Ala1415Pro