Canonical Allele Identifier: CA394884856
Gene: ABCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16169778G>A , CM000678.2:g.16169778G>A GRCh38
NC_000016.9:g.16263635G>A , CM000678.1:g.16263635G>A GRCh37
NC_000016.8:g.16171136G>A NCBI36
NG_007558.2:g.58694C>T
NG_007558.3:g.58840C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.2863C>T ENSP00000483331.2:p.Leu955Phe
ENST00000205557.12:c.2863C>T MANE Select ENSP00000205557.7:p.Leu955Phe
ENST00000205557.11:c.2863C>T ENSP00000205557.7:p.Leu955Phe
ENST00000456970.6:c.2688C>T ENSP00000405002.2:n.2688C>T
ENST00000622290.4:c.*72C>T ENSP00000483331.1:n.*72C>T
NM_001171.5:c.2863C>T NP_001162.4:p.Leu955Phe
XM_011522479.1:c.2830C>T XP_011520781.1:p.Leu944Phe
XM_011522480.1:c.2521C>T XP_011520782.1:p.Leu841Phe
XM_011522481.1:c.2521C>T XP_011520783.1:p.Leu841Phe
XR_932836.1:n.3098C>T
XR_932837.1:n.3099C>T
XR_932838.1:n.3099C>T
NM_001351800.1:c.2521C>T NP_001338729.1:p.Leu841Phe
NR_147784.1:n.2725C>T
XM_011522479.2:c.2830C>T XP_011520781.1:p.Leu944Phe
XM_011522481.3:c.2521C>T XP_011520783.1:p.Leu841Phe
XM_017023212.1:c.2695C>T XP_016878701.1:p.Leu899Phe
XM_017023214.1:c.2863C>T XP_016878703.1:p.Leu955Phe
XM_024450261.1:c.2899C>T XP_024306029.1:p.Leu967Phe
XR_932836.2:n.3044C>T
XR_932837.3:n.3044C>T
XR_932838.3:n.3044C>T
NM_001171.6:c.2863C>T MANE Select NP_001162.5:p.Leu955Phe