Canonical Allele Identifier: CA394880537

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16256892T>A (hg19) ; chr16:g.16163035T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16163035T>A , CM000678.2:g.16163035T>A	GRCh38
NC_000016.9:g.16256892T>A , CM000678.1:g.16256892T>A	GRCh37
NC_000016.8:g.16164393T>A	NCBI36
NG_007558.2:g.65437A>T
NG_007558.3:g.65583A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3464A>T	ENSP00000483331.2:p.Asp1155Val
ENST00000205557.12:c.3464A>T MANE Select	ENSP00000205557.7:p.Asp1155Val
ENST00000640696.1:c.321-1471A>T	ENSP00000492197.1:n.321-1471A>T
ENST00000205557.11:c.3464A>T	ENSP00000205557.7:p.Asp1155Val
ENST00000456970.6:c.3132-1471A>T	ENSP00000405002.2:n.3132-1471A>T
ENST00000622290.4:c.*673A>T	ENSP00000483331.1:n.*673A>T
NM_001171.5:c.3464A>T	NP_001162.4:p.Asp1155Val
XM_011522479.1:c.3431A>T	XP_011520781.1:p.Asp1144Val
XM_011522480.1:c.3122A>T	XP_011520782.1:p.Asp1041Val
XM_011522481.1:c.3122A>T	XP_011520783.1:p.Asp1041Val
XR_932836.1:n.3699A>T
XR_932837.1:n.3543-1471A>T
XR_932838.1:n.3543-1471A>T
XR_933133.1:n.407+192T>A
XR_933134.1:n.754+192T>A
NM_001351800.1:c.3122A>T	NP_001338729.1:p.Asp1041Val
NR_147784.1:n.3169-1471A>T
XM_011522479.2:c.3431A>T	XP_011520781.1:p.Asp1144Val
XM_011522481.3:c.3122A>T	XP_011520783.1:p.Asp1041Val
XM_017023212.1:c.3296A>T	XP_016878701.1:p.Asp1099Val
XM_017023214.1:c.3307-1471A>T	XP_016878703.1:n.3307-1471A>T
XM_024450261.1:c.3500A>T	XP_024306029.1:p.Asp1167Val
XR_932836.2:n.3645A>T
XR_932837.3:n.3488-1471A>T
XR_932838.3:n.3488-1471A>T
NM_001171.6:c.3464A>T MANE Select	NP_001162.5:p.Asp1155Val