Canonical Allele Identifier: CA394875437

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16248743C>G (hg19) ; chr16:g.16154886C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154886C>G , CM000678.2:g.16154886C>G	GRCh38
NC_000016.9:g.16248743C>G , CM000678.1:g.16248743C>G	GRCh37
NC_000016.8:g.16156244C>G	NCBI36
NG_007558.2:g.73586G>C
NG_007558.3:g.73732G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.891G>C
ENST00000622290.5:c.*200G>C	ENSP00000483331.2:n.*200G>C
ENST00000205557.12:c.4028G>C MANE Select	ENSP00000205557.7:p.Ser1343Thr
ENST00000640696.1:c.842G>C	ENSP00000492197.1:p.Ser281Thr
ENST00000205557.11:c.4028G>C	ENSP00000205557.7:p.Ser1343Thr
ENST00000456970.6:c.3653G>C	ENSP00000405002.2:n.3653G>C
ENST00000576204.5:n.891G>C
ENST00000622290.4:c.*1237G>C	ENSP00000483331.1:n.*1237G>C
NM_001171.5:c.4028G>C	NP_001162.4:p.Ser1343Thr
XM_011522479.1:c.3995G>C	XP_011520781.1:p.Ser1332Thr
XM_011522480.1:c.3686G>C	XP_011520782.1:p.Ser1229Thr
XM_011522481.1:c.3686G>C	XP_011520783.1:p.Ser1229Thr
XR_933134.1:n.539-4895C>G
NM_001351800.1:c.3686G>C	NP_001338729.1:p.Ser1229Thr
NR_147784.1:n.3690G>C
XM_011522479.2:c.3995G>C	XP_011520781.1:p.Ser1332Thr
XM_011522481.3:c.3686G>C	XP_011520783.1:p.Ser1229Thr
XM_017023212.1:c.3860G>C	XP_016878701.1:p.Ser1287Thr
XM_024450261.1:c.4064G>C	XP_024306029.1:p.Ser1355Thr
NM_001171.6:c.4028G>C MANE Select	NP_001162.5:p.Ser1343Thr