Canonical Allele Identifier: CA394884249

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16263510A>T (hg19) ; chr16:g.16169653A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169653A>T , CM000678.2:g.16169653A>T	GRCh38
NC_000016.9:g.16263510A>T , CM000678.1:g.16263510A>T	GRCh37
NC_000016.8:g.16171011A>T	NCBI36
NG_007558.2:g.58819T>A
NG_007558.3:g.58965T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2988T>A	ENSP00000483331.2:p.Cys996Ter
ENST00000205557.12:c.2988T>A MANE Select	ENSP00000205557.7:p.Cys996Ter
ENST00000205557.11:c.2988T>A	ENSP00000205557.7:p.Cys996Ter
ENST00000456970.6:c.2813T>A	ENSP00000405002.2:n.2813T>A
ENST00000622290.4:c.*197T>A	ENSP00000483331.1:n.*197T>A
NM_001171.5:c.2988T>A	NP_001162.4:p.Cys996Ter
XM_011522479.1:c.2955T>A	XP_011520781.1:p.Cys985Ter
XM_011522480.1:c.2646T>A	XP_011520782.1:p.Cys882Ter
XM_011522481.1:c.2646T>A	XP_011520783.1:p.Cys882Ter
XR_932836.1:n.3223T>A
XR_932837.1:n.3224T>A
XR_932838.1:n.3224T>A
NM_001351800.1:c.2646T>A	NP_001338729.1:p.Cys882Ter
NR_147784.1:n.2850T>A
XM_011522479.2:c.2955T>A	XP_011520781.1:p.Cys985Ter
XM_011522481.3:c.2646T>A	XP_011520783.1:p.Cys882Ter
XM_017023212.1:c.2820T>A	XP_016878701.1:p.Cys940Ter
XM_017023214.1:c.2988T>A	XP_016878703.1:p.Cys996Ter
XM_024450261.1:c.3024T>A	XP_024306029.1:p.Cys1008Ter
XR_932836.2:n.3169T>A
XR_932837.3:n.3169T>A
XR_932838.3:n.3169T>A
NM_001171.6:c.2988T>A MANE Select	NP_001162.5:p.Cys996Ter