Canonical Allele Identifier: CA394883745

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16244475G>T (hg19) ; chr16:g.16150618G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150618G>T , CM000678.2:g.16150618G>T	GRCh38
NC_000016.9:g.16244475G>T , CM000678.1:g.16244475G>T	GRCh37
NC_000016.8:g.16151976G>T	NCBI36
NG_007558.2:g.77854C>A
NG_007558.3:g.78000C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*535C>A	ENSP00000483331.2:n.*535C>A
ENST00000205557.12:c.4363C>A MANE Select	ENSP00000205557.7:p.Leu1455Ile
ENST00000640696.1:c.1177C>A	ENSP00000492197.1:p.Leu393Ile
ENST00000205557.11:c.4363C>A	ENSP00000205557.7:p.Leu1455Ile
ENST00000456970.6:c.3988C>A	ENSP00000405002.2:n.3988C>A
ENST00000576204.5:n.1226C>A
ENST00000622290.4:c.*1572C>A	ENSP00000483331.1:n.*1572C>A
NM_001171.5:c.4363C>A	NP_001162.4:p.Leu1455Ile
XM_011522479.1:c.4330C>A	XP_011520781.1:p.Leu1444Ile
XM_011522480.1:c.4021C>A	XP_011520782.1:p.Leu1341Ile
XM_011522481.1:c.4021C>A	XP_011520783.1:p.Leu1341Ile
XR_933134.1:n.538+6328G>T
NM_001351800.1:c.4021C>A	NP_001338729.1:p.Leu1341Ile
NR_147784.1:n.4025C>A
XM_011522479.2:c.4330C>A	XP_011520781.1:p.Leu1444Ile
XM_011522481.3:c.4021C>A	XP_011520783.1:p.Leu1341Ile
XM_017023212.1:c.4195C>A	XP_016878701.1:p.Leu1399Ile
XM_024450261.1:c.4399C>A	XP_024306029.1:p.Leu1467Ile
NM_001171.6:c.4363C>A MANE Select	NP_001162.5:p.Leu1455Ile