Canonical Allele Identifier: CA394883028

Gene: ABCC6

Linked Data

• MyVariant Identifiers: chr16:g.16259587G>T (hg19) ; chr16:g.16165730G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16165730G>T , CM000678.2:g.16165730G>T	GRCh38
NC_000016.9:g.16259587G>T , CM000678.1:g.16259587G>T	GRCh37
NC_000016.8:g.16167088G>T	NCBI36
NG_007558.2:g.62742C>A
NG_007558.3:g.62888C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000622290.5:c.3199C>A	ENSP00000483331.2:p.Leu1067Met
ENST00000205557.12:c.3199C>A MANE Select	ENSP00000205557.7:p.Leu1067Met
ENST00000640696.1:c.214C>A	ENSP00000492197.1:p.Leu72Met
ENST00000205557.11:c.3199C>A	ENSP00000205557.7:p.Leu1067Met
ENST00000456970.6:c.3024C>A	ENSP00000405002.2:n.3024C>A
ENST00000622290.4:c.*408C>A	ENSP00000483331.1:n.*408C>A
NM_001171.5:c.3199C>A	NP_001162.4:p.Leu1067Met
XM_011522479.1:c.3166C>A	XP_011520781.1:p.Leu1056Met
XM_011522480.1:c.2857C>A	XP_011520782.1:p.Leu953Met
XM_011522481.1:c.2857C>A	XP_011520783.1:p.Leu953Met
XR_932836.1:n.3434C>A
XR_932837.1:n.3435C>A
XR_932838.1:n.3435C>A
NM_001351800.1:c.2857C>A	NP_001338729.1:p.Leu953Met
NR_147784.1:n.3061C>A
XM_011522479.2:c.3166C>A	XP_011520781.1:p.Leu1056Met
XM_011522481.3:c.2857C>A	XP_011520783.1:p.Leu953Met
XM_017023212.1:c.3031C>A	XP_016878701.1:p.Leu1011Met
XM_017023214.1:c.3199C>A	XP_016878703.1:p.Leu1067Met
XM_024450261.1:c.3235C>A	XP_024306029.1:p.Leu1079Met
XR_932836.2:n.3380C>A
XR_932837.3:n.3380C>A
XR_932838.3:n.3380C>A
NM_001171.6:c.3199C>A MANE Select	NP_001162.5:p.Leu1067Met