Canonical Allele Identifier: CA394883733

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16244470A>C (hg19) ; chr16:g.16150613A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150613A>C , CM000678.2:g.16150613A>C	GRCh38
NC_000016.9:g.16244470A>C , CM000678.1:g.16244470A>C	GRCh37
NC_000016.8:g.16151971A>C	NCBI36
NG_007558.2:g.77859T>G
NG_007558.3:g.78005T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000622290.5:c.*540T>G	ENSP00000483331.2:n.*540T>G
ENST00000205557.12:c.4368T>G MANE Select	ENSP00000205557.7:p.Ile1456Met
ENST00000640696.1:c.1182T>G	ENSP00000492197.1:p.Ile394Met
ENST00000205557.11:c.4368T>G	ENSP00000205557.7:p.Ile1456Met
ENST00000456970.6:c.3993T>G	ENSP00000405002.2:n.3993T>G
ENST00000576204.5:n.1231T>G
ENST00000622290.4:c.*1577T>G	ENSP00000483331.1:n.*1577T>G
NM_001171.5:c.4368T>G	NP_001162.4:p.Ile1456Met
XM_011522479.1:c.4335T>G	XP_011520781.1:p.Ile1445Met
XM_011522480.1:c.4026T>G	XP_011520782.1:p.Ile1342Met
XM_011522481.1:c.4026T>G	XP_011520783.1:p.Ile1342Met
XR_933134.1:n.538+6323A>C
NM_001351800.1:c.4026T>G	NP_001338729.1:p.Ile1342Met
NR_147784.1:n.4030T>G
XM_011522479.2:c.4335T>G	XP_011520781.1:p.Ile1445Met
XM_011522481.3:c.4026T>G	XP_011520783.1:p.Ile1342Met
XM_017023212.1:c.4200T>G	XP_016878701.1:p.Ile1400Met
XM_024450261.1:c.4404T>G	XP_024306029.1:p.Ile1468Met
NM_001171.6:c.4368T>G MANE Select	NP_001162.5:p.Ile1456Met