Canonical Allele Identifier: CA394890421
Gene: ABCC6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16198160G>C , CM000678.2:g.16198160G>C GRCh38
NC_000016.9:g.16292017G>C , CM000678.1:g.16292017G>C GRCh37
NC_000016.8:g.16199518G>C NCBI36
NG_007558.2:g.30312C>G
NG_007558.3:g.30458C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000574094.6:c.1199C>G ENSP00000507301.1:p.Ser400Cys
ENST00000622290.5:c.1199C>G ENSP00000483331.2:p.Ser400Cys
ENST00000205557.12:c.1199C>G MANE Select ENSP00000205557.7:p.Ser400Cys
ENST00000205557.11:c.1199C>G ENSP00000205557.7:p.Ser400Cys
ENST00000456970.6:c.1199C>G ENSP00000405002.2:p.Ser400Cys
ENST00000574094.5:n.1295C>G
ENST00000622290.4:c.1199C>G ENSP00000483331.1:p.Ser400Cys
NM_001171.5:c.1199C>G NP_001162.4:p.Ser400Cys
XM_011522479.1:c.1199C>G XP_011520781.1:p.Ser400Cys
XM_011522480.1:c.857C>G XP_011520782.1:p.Ser286Cys
XM_011522481.1:c.857C>G XP_011520783.1:p.Ser286Cys
XM_011522482.1:c.1199C>G XP_011520784.1:p.Ser400Cys
XR_932836.1:n.1434C>G
XR_932837.1:n.1435C>G
XR_932838.1:n.1435C>G
NM_001351800.1:c.857C>G NP_001338729.1:p.Ser286Cys
NR_147784.1:n.1236C>G
XM_011522479.2:c.1199C>G XP_011520781.1:p.Ser400Cys
XM_011522481.3:c.857C>G XP_011520783.1:p.Ser286Cys
XM_011522482.3:c.1199C>G XP_011520784.1:p.Ser400Cys
XM_017023212.1:c.1199C>G XP_016878701.1:p.Ser400Cys
XM_017023214.1:c.1199C>G XP_016878703.1:p.Ser400Cys
XM_024450261.1:c.1235C>G XP_024306029.1:p.Ser412Cys
XR_932836.2:n.1380C>G
XR_932837.3:n.1380C>G
XR_932838.3:n.1380C>G
NM_001171.6:c.1199C>G MANE Select NP_001162.5:p.Ser400Cys