Canonical Allele Identifier: CA394884833

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16248644A>T (hg19) ; chr16:g.16154787A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16154787A>T , CM000678.2:g.16154787A>T	GRCh38
NC_000016.9:g.16248644A>T , CM000678.1:g.16248644A>T	GRCh37
NC_000016.8:g.16156145A>T	NCBI36
NG_007558.2:g.73685T>A
NG_007558.3:g.73831T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000576204.6:n.912T>A
ENST00000622290.5:c.*221T>A	ENSP00000483331.2:n.*221T>A
ENST00000205557.12:c.4049T>A MANE Select	ENSP00000205557.7:p.Ile1350Asn
ENST00000640696.1:c.863T>A	ENSP00000492197.1:p.Ile288Asn
ENST00000205557.11:c.4049T>A	ENSP00000205557.7:p.Ile1350Asn
ENST00000456970.6:c.3674T>A	ENSP00000405002.2:n.3674T>A
ENST00000576204.5:n.912T>A
ENST00000622290.4:c.*1258T>A	ENSP00000483331.1:n.*1258T>A
NM_001171.5:c.4049T>A	NP_001162.4:p.Ile1350Asn
XM_011522479.1:c.4016T>A	XP_011520781.1:p.Ile1339Asn
XM_011522480.1:c.3707T>A	XP_011520782.1:p.Ile1236Asn
XM_011522481.1:c.3707T>A	XP_011520783.1:p.Ile1236Asn
XR_933134.1:n.539-4994A>T
NM_001351800.1:c.3707T>A	NP_001338729.1:p.Ile1236Asn
NR_147784.1:n.3711T>A
XM_011522479.2:c.4016T>A	XP_011520781.1:p.Ile1339Asn
XM_011522481.3:c.3707T>A	XP_011520783.1:p.Ile1236Asn
XM_017023212.1:c.3881T>A	XP_016878701.1:p.Ile1294Asn
XM_024450261.1:c.4085T>A	XP_024306029.1:p.Ile1362Asn
NM_001171.6:c.4049T>A MANE Select	NP_001162.5:p.Ile1350Asn