Canonical Allele Identifier: CA394884916
Gene: ABCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16169799G>A , CM000678.2:g.16169799G>A GRCh38
NC_000016.9:g.16263656G>A , CM000678.1:g.16263656G>A GRCh37
NC_000016.8:g.16171157G>A NCBI36
NG_007558.2:g.58673C>T
NG_007558.3:g.58819C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.2842C>T ENSP00000483331.2:p.Leu948Phe
ENST00000205557.12:c.2842C>T MANE Select ENSP00000205557.7:p.Leu948Phe
ENST00000205557.11:c.2842C>T ENSP00000205557.7:p.Leu948Phe
ENST00000456970.6:c.2667C>T ENSP00000405002.2:n.2667C>T
ENST00000622290.4:c.*51C>T ENSP00000483331.1:n.*51C>T
NM_001171.5:c.2842C>T NP_001162.4:p.Leu948Phe
XM_011522479.1:c.2809C>T XP_011520781.1:p.Leu937Phe
XM_011522480.1:c.2500C>T XP_011520782.1:p.Leu834Phe
XM_011522481.1:c.2500C>T XP_011520783.1:p.Leu834Phe
XR_932836.1:n.3077C>T
XR_932837.1:n.3078C>T
XR_932838.1:n.3078C>T
NM_001351800.1:c.2500C>T NP_001338729.1:p.Leu834Phe
NR_147784.1:n.2704C>T
XM_011522479.2:c.2809C>T XP_011520781.1:p.Leu937Phe
XM_011522481.3:c.2500C>T XP_011520783.1:p.Leu834Phe
XM_017023212.1:c.2674C>T XP_016878701.1:p.Leu892Phe
XM_017023214.1:c.2842C>T XP_016878703.1:p.Leu948Phe
XM_024450261.1:c.2878C>T XP_024306029.1:p.Leu960Phe
XR_932836.2:n.3023C>T
XR_932837.3:n.3023C>T
XR_932838.3:n.3023C>T
NM_001171.6:c.2842C>T MANE Select NP_001162.5:p.Leu948Phe