Canonical Allele Identifier: CA394890410
Gene: ABCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16198154T>G , CM000678.2:g.16198154T>G GRCh38
NC_000016.9:g.16292011T>G , CM000678.1:g.16292011T>G GRCh37
NC_000016.8:g.16199512T>G NCBI36
NG_007558.2:g.30318A>C
NG_007558.3:g.30464A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000574094.6:c.1205A>C ENSP00000507301.1:p.Lys402Thr
ENST00000622290.5:c.1205A>C ENSP00000483331.2:p.Lys402Thr
ENST00000205557.12:c.1205A>C MANE Select ENSP00000205557.7:p.Lys402Thr
ENST00000205557.11:c.1205A>C ENSP00000205557.7:p.Lys402Thr
ENST00000456970.6:c.1205A>C ENSP00000405002.2:p.Lys402Thr
ENST00000574094.5:n.1301A>C
ENST00000622290.4:c.1205A>C ENSP00000483331.1:p.Lys402Thr
NM_001171.5:c.1205A>C NP_001162.4:p.Lys402Thr
XM_011522479.1:c.1205A>C XP_011520781.1:p.Lys402Thr
XM_011522480.1:c.863A>C XP_011520782.1:p.Lys288Thr
XM_011522481.1:c.863A>C XP_011520783.1:p.Lys288Thr
XM_011522482.1:c.1205A>C XP_011520784.1:p.Lys402Thr
XR_932836.1:n.1440A>C
XR_932837.1:n.1441A>C
XR_932838.1:n.1441A>C
NM_001351800.1:c.863A>C NP_001338729.1:p.Lys288Thr
NR_147784.1:n.1242A>C
XM_011522479.2:c.1205A>C XP_011520781.1:p.Lys402Thr
XM_011522481.3:c.863A>C XP_011520783.1:p.Lys288Thr
XM_011522482.3:c.1205A>C XP_011520784.1:p.Lys402Thr
XM_017023212.1:c.1205A>C XP_016878701.1:p.Lys402Thr
XM_017023214.1:c.1205A>C XP_016878703.1:p.Lys402Thr
XM_024450261.1:c.1241A>C XP_024306029.1:p.Lys414Thr
XR_932836.2:n.1386A>C
XR_932837.3:n.1386A>C
XR_932838.3:n.1386A>C
NM_001171.6:c.1205A>C MANE Select NP_001162.5:p.Lys402Thr