Canonical Allele Identifier: CA394878873

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16253416C>A (hg19) ; chr16:g.16159559C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159559C>A , CM000678.2:g.16159559C>A	GRCh38
NC_000016.9:g.16253416C>A , CM000678.1:g.16253416C>A	GRCh37
NC_000016.8:g.16160917C>A	NCBI36
NG_007558.2:g.68913G>T
NG_007558.3:g.69059G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000622290.5:c.3658G>T	ENSP00000483331.2:p.Val1220Phe
ENST00000205557.12:c.3658G>T MANE Select	ENSP00000205557.7:p.Val1220Phe
ENST00000640696.1:c.472G>T	ENSP00000492197.1:p.Val158Phe
ENST00000205557.11:c.3658G>T	ENSP00000205557.7:p.Val1220Phe
ENST00000456970.6:c.3283G>T	ENSP00000405002.2:n.3283G>T
ENST00000622290.4:c.*867G>T	ENSP00000483331.1:n.*867G>T
NM_001171.5:c.3658G>T	NP_001162.4:p.Val1220Phe
XM_011522479.1:c.3625G>T	XP_011520781.1:p.Val1209Phe
XM_011522480.1:c.3316G>T	XP_011520782.1:p.Val1106Phe
XM_011522481.1:c.3316G>T	XP_011520783.1:p.Val1106Phe
XR_932836.1:n.3893G>T
XR_932837.1:n.3694G>T
XR_932838.1:n.3694G>T
XR_933134.1:n.539-222C>A
NM_001351800.1:c.3316G>T	NP_001338729.1:p.Val1106Phe
NR_147784.1:n.3320G>T
XM_011522479.2:c.3625G>T	XP_011520781.1:p.Val1209Phe
XM_011522481.3:c.3316G>T	XP_011520783.1:p.Val1106Phe
XM_017023212.1:c.3490G>T	XP_016878701.1:p.Val1164Phe
XM_024450261.1:c.3694G>T	XP_024306029.1:p.Val1232Phe
XR_932836.2:n.3839G>T
XR_932837.3:n.3639G>T
XR_932838.3:n.3639G>T
NM_001171.6:c.3658G>T MANE Select	NP_001162.5:p.Val1220Phe