Canonical Allele Identifier: CA394875417

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16248740A>G (hg19) ; chr16:g.16154883A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154883A>G , CM000678.2:g.16154883A>G	GRCh38
NC_000016.9:g.16248740A>G , CM000678.1:g.16248740A>G	GRCh37
NC_000016.8:g.16156241A>G	NCBI36
NG_007558.2:g.73589T>C
NG_007558.3:g.73735T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.894T>C
ENST00000622290.5:c.*203T>C	ENSP00000483331.2:n.*203T>C
ENST00000205557.12:c.4031T>C MANE Select	ENSP00000205557.7:p.Ile1344Thr
ENST00000640696.1:c.845T>C	ENSP00000492197.1:p.Ile282Thr
ENST00000205557.11:c.4031T>C	ENSP00000205557.7:p.Ile1344Thr
ENST00000456970.6:c.3656T>C	ENSP00000405002.2:n.3656T>C
ENST00000576204.5:n.894T>C
ENST00000622290.4:c.*1240T>C	ENSP00000483331.1:n.*1240T>C
NM_001171.5:c.4031T>C	NP_001162.4:p.Ile1344Thr
XM_011522479.1:c.3998T>C	XP_011520781.1:p.Ile1333Thr
XM_011522480.1:c.3689T>C	XP_011520782.1:p.Ile1230Thr
XM_011522481.1:c.3689T>C	XP_011520783.1:p.Ile1230Thr
XR_933134.1:n.539-4898A>G
NM_001351800.1:c.3689T>C	NP_001338729.1:p.Ile1230Thr
NR_147784.1:n.3693T>C
XM_011522479.2:c.3998T>C	XP_011520781.1:p.Ile1333Thr
XM_011522481.3:c.3689T>C	XP_011520783.1:p.Ile1230Thr
XM_017023212.1:c.3863T>C	XP_016878701.1:p.Ile1288Thr
XM_024450261.1:c.4067T>C	XP_024306029.1:p.Ile1356Thr
NM_001171.6:c.4031T>C MANE Select	NP_001162.5:p.Ile1344Thr