Canonical Allele Identifier: CA493801136

Gene: ABCC6

Linked Data

• COSMIC: COSM6143377
• MyVariant Identifiers: chr16:g.16297269G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16203412G>A , CM000678.2:g.16203412G>A	GRCh38
NC_000016.9:g.16297269G>A , CM000678.1:g.16297269G>A	GRCh37
NC_000016.8:g.16204770G>A	NCBI36
NG_007558.2:g.25060C>T
NG_007558.3:g.25206C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574094.6:c.996C>T	ENSP00000507301.1:p.Leu332=
ENST00000622290.5:c.996C>T	ENSP00000483331.2:p.Leu332=
ENST00000205557.12:c.996C>T MANE Select	ENSP00000205557.7:p.Leu332=
ENST00000205557.11:c.996C>T	ENSP00000205557.7:p.Leu332=
ENST00000456970.6:c.996C>T	ENSP00000405002.2:p.Leu332=
ENST00000574094.5:n.1092C>T
ENST00000577103.1:c.*863C>T	ENSP00000459243.1:n.*863C>T
ENST00000622290.4:c.996C>T	ENSP00000483331.1:p.Leu332=
NM_001171.5:c.996C>T	NP_001162.4:p.Leu332=
XM_011522479.1:c.996C>T	XP_011520781.1:p.Leu332=
XM_011522480.1:c.654C>T	XP_011520782.1:p.Leu218=
XM_011522481.1:c.654C>T	XP_011520783.1:p.Leu218=
XM_011522482.1:c.996C>T	XP_011520784.1:p.Leu332=
XR_932836.1:n.1231C>T
XR_932837.1:n.1232C>T
XR_932838.1:n.1232C>T
NM_001351800.1:c.654C>T	NP_001338729.1:p.Leu218=
NR_147784.1:n.1033C>T
XM_011522479.2:c.996C>T	XP_011520781.1:p.Leu332=
XM_011522481.3:c.654C>T	XP_011520783.1:p.Leu218=
XM_011522482.3:c.996C>T	XP_011520784.1:p.Leu332=
XM_017023212.1:c.996C>T	XP_016878701.1:p.Leu332=
XM_017023214.1:c.996C>T	XP_016878703.1:p.Leu332=
XM_024450261.1:c.1032C>T	XP_024306029.1:p.Leu344=
XR_932836.2:n.1177C>T
XR_932837.3:n.1177C>T
XR_932838.3:n.1177C>T
NM_001171.6:c.996C>T MANE Select	NP_001162.5:p.Leu332=