Canonical Allele Identifier: CA394878829

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16253406C>G (hg19) ; chr16:g.16159549C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159549C>G , CM000678.2:g.16159549C>G	GRCh38
NC_000016.9:g.16253406C>G , CM000678.1:g.16253406C>G	GRCh37
NC_000016.8:g.16160907C>G	NCBI36
NG_007558.2:g.68923G>C
NG_007558.3:g.69069G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000622290.5:c.3668G>C	ENSP00000483331.2:p.Trp1223Ser
ENST00000205557.12:c.3668G>C MANE Select	ENSP00000205557.7:p.Trp1223Ser
ENST00000640696.1:c.482G>C	ENSP00000492197.1:p.Trp161Ser
ENST00000205557.11:c.3668G>C	ENSP00000205557.7:p.Trp1223Ser
ENST00000456970.6:c.3293G>C	ENSP00000405002.2:n.3293G>C
ENST00000622290.4:c.*877G>C	ENSP00000483331.1:n.*877G>C
NM_001171.5:c.3668G>C	NP_001162.4:p.Trp1223Ser
XM_011522479.1:c.3635G>C	XP_011520781.1:p.Trp1212Ser
XM_011522480.1:c.3326G>C	XP_011520782.1:p.Trp1109Ser
XM_011522481.1:c.3326G>C	XP_011520783.1:p.Trp1109Ser
XR_932836.1:n.3903G>C
XR_932837.1:n.3704G>C
XR_932838.1:n.3704G>C
XR_933134.1:n.539-232C>G
NM_001351800.1:c.3326G>C	NP_001338729.1:p.Trp1109Ser
NR_147784.1:n.3330G>C
XM_011522479.2:c.3635G>C	XP_011520781.1:p.Trp1212Ser
XM_011522481.3:c.3326G>C	XP_011520783.1:p.Trp1109Ser
XM_017023212.1:c.3500G>C	XP_016878701.1:p.Trp1167Ser
XM_024450261.1:c.3704G>C	XP_024306029.1:p.Trp1235Ser
XR_932836.2:n.3849G>C
XR_932837.3:n.3649G>C
XR_932838.3:n.3649G>C
NM_001171.6:c.3668G>C MANE Select	NP_001162.5:p.Trp1223Ser