Canonical Allele Identifier: CA394880496

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16256886C>G (hg19) ; chr16:g.16163029C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16163029C>G , CM000678.2:g.16163029C>G	GRCh38
NC_000016.9:g.16256886C>G , CM000678.1:g.16256886C>G	GRCh37
NC_000016.8:g.16164387C>G	NCBI36
NG_007558.2:g.65443G>C
NG_007558.3:g.65589G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3470G>C	ENSP00000483331.2:p.Ser1157Thr
ENST00000205557.12:c.3470G>C MANE Select	ENSP00000205557.7:p.Ser1157Thr
ENST00000640696.1:c.321-1465G>C	ENSP00000492197.1:n.321-1465G>C
ENST00000205557.11:c.3470G>C	ENSP00000205557.7:p.Ser1157Thr
ENST00000456970.6:c.3132-1465G>C	ENSP00000405002.2:n.3132-1465G>C
ENST00000622290.4:c.*679G>C	ENSP00000483331.1:n.*679G>C
NM_001171.5:c.3470G>C	NP_001162.4:p.Ser1157Thr
XM_011522479.1:c.3437G>C	XP_011520781.1:p.Ser1146Thr
XM_011522480.1:c.3128G>C	XP_011520782.1:p.Ser1043Thr
XM_011522481.1:c.3128G>C	XP_011520783.1:p.Ser1043Thr
XR_932836.1:n.3705G>C
XR_932837.1:n.3543-1465G>C
XR_932838.1:n.3543-1465G>C
XR_933133.1:n.407+186C>G
XR_933134.1:n.754+186C>G
NM_001351800.1:c.3128G>C	NP_001338729.1:p.Ser1043Thr
NR_147784.1:n.3169-1465G>C
XM_011522479.2:c.3437G>C	XP_011520781.1:p.Ser1146Thr
XM_011522481.3:c.3128G>C	XP_011520783.1:p.Ser1043Thr
XM_017023212.1:c.3302G>C	XP_016878701.1:p.Ser1101Thr
XM_017023214.1:c.3307-1465G>C	XP_016878703.1:n.3307-1465G>C
XM_024450261.1:c.3506G>C	XP_024306029.1:p.Ser1169Thr
XR_932836.2:n.3651G>C
XR_932837.3:n.3488-1465G>C
XR_932838.3:n.3488-1465G>C
NM_001171.6:c.3470G>C MANE Select	NP_001162.5:p.Ser1157Thr