Canonical Allele Identifier: CA394890249
Gene: ABCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16198070A>G , CM000678.2:g.16198070A>G GRCh38
NC_000016.9:g.16291927A>G , CM000678.1:g.16291927A>G GRCh37
NC_000016.8:g.16199428A>G NCBI36
NG_007558.2:g.30402T>C
NG_007558.3:g.30548T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000574094.6:c.1289T>C ENSP00000507301.1:p.Leu430Pro
ENST00000622290.5:c.1289T>C ENSP00000483331.2:p.Leu430Pro
ENST00000205557.12:c.1289T>C MANE Select ENSP00000205557.7:p.Leu430Pro
ENST00000205557.11:c.1289T>C ENSP00000205557.7:p.Leu430Pro
ENST00000456970.6:c.1289T>C ENSP00000405002.2:p.Leu430Pro
ENST00000574094.5:n.1385T>C
ENST00000622290.4:c.1289T>C ENSP00000483331.1:p.Leu430Pro
NM_001171.5:c.1289T>C NP_001162.4:p.Leu430Pro
XM_011522479.1:c.1289T>C XP_011520781.1:p.Leu430Pro
XM_011522480.1:c.947T>C XP_011520782.1:p.Leu316Pro
XM_011522481.1:c.947T>C XP_011520783.1:p.Leu316Pro
XM_011522482.1:c.1289T>C XP_011520784.1:p.Leu430Pro
XR_932836.1:n.1524T>C
XR_932837.1:n.1525T>C
XR_932838.1:n.1525T>C
NM_001351800.1:c.947T>C NP_001338729.1:p.Leu316Pro
NR_147784.1:n.1326T>C
XM_011522479.2:c.1289T>C XP_011520781.1:p.Leu430Pro
XM_011522481.3:c.947T>C XP_011520783.1:p.Leu316Pro
XM_011522482.3:c.1289T>C XP_011520784.1:p.Leu430Pro
XM_017023212.1:c.1289T>C XP_016878701.1:p.Leu430Pro
XM_017023214.1:c.1289T>C XP_016878703.1:p.Leu430Pro
XM_024450261.1:c.1325T>C XP_024306029.1:p.Leu442Pro
XR_932836.2:n.1470T>C
XR_932837.3:n.1470T>C
XR_932838.3:n.1470T>C
NM_001171.6:c.1289T>C MANE Select NP_001162.5:p.Leu430Pro