Canonical Allele Identifier: CA493799332

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16263519G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169662G>T , CM000678.2:g.16169662G>T	GRCh38
NC_000016.9:g.16263519G>T , CM000678.1:g.16263519G>T	GRCh37
NC_000016.8:g.16171020G>T	NCBI36
NG_007558.2:g.58810C>A
NG_007558.3:g.58956C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2979C>A	ENSP00000483331.2:p.Leu993=
ENST00000205557.12:c.2979C>A MANE Select	ENSP00000205557.7:p.Leu993=
ENST00000205557.11:c.2979C>A	ENSP00000205557.7:p.Leu993=
ENST00000456970.6:c.2804C>A	ENSP00000405002.2:n.2804C>A
ENST00000622290.4:c.*188C>A	ENSP00000483331.1:n.*188C>A
NM_001171.5:c.2979C>A	NP_001162.4:p.Leu993=
XM_011522479.1:c.2946C>A	XP_011520781.1:p.Leu982=
XM_011522480.1:c.2637C>A	XP_011520782.1:p.Leu879=
XM_011522481.1:c.2637C>A	XP_011520783.1:p.Leu879=
XR_932836.1:n.3214C>A
XR_932837.1:n.3215C>A
XR_932838.1:n.3215C>A
NM_001351800.1:c.2637C>A	NP_001338729.1:p.Leu879=
NR_147784.1:n.2841C>A
XM_011522479.2:c.2946C>A	XP_011520781.1:p.Leu982=
XM_011522481.3:c.2637C>A	XP_011520783.1:p.Leu879=
XM_017023212.1:c.2811C>A	XP_016878701.1:p.Leu937=
XM_017023214.1:c.2979C>A	XP_016878703.1:p.Leu993=
XM_024450261.1:c.3015C>A	XP_024306029.1:p.Leu1005=
XR_932836.2:n.3160C>A
XR_932837.3:n.3160C>A
XR_932838.3:n.3160C>A
NM_001171.6:c.2979C>A MANE Select	NP_001162.5:p.Leu993=