Canonical Allele Identifier: CA2210139933
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16165736A= , CM000678.2:g.16165736A= GRCh38
NC_000016.9:g.16259593A= , CM000678.1:g.16259593A= GRCh37
NC_000016.8:g.16167094A= NCBI36
NG_007558.2:g.62736T=
NG_007558.3:g.62882T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.3193T= ENSP00000483331.2:p.Ser1065=
ENST00000205557.12:c.3193T= MANE Select ENSP00000205557.7:p.Ser1065=
ENST00000640696.1:c.208T= ENSP00000492197.1:p.Ser70=
ENST00000205557.11:c.3193T= ENSP00000205557.7:p.Ser1065=
ENST00000456970.6:c.3018T= ENSP00000405002.2:n.3018T=
ENST00000622290.4:c.*402T= ENSP00000483331.1:n.*402T=
NM_001171.5:c.3193T= NP_001162.4:p.Ser1065=
XM_011522479.1:c.3160T= XP_011520781.1:p.Ser1054=
XM_011522480.1:c.2851T= XP_011520782.1:p.Ser951=
XM_011522481.1:c.2851T= XP_011520783.1:p.Ser951=
XR_932836.1:n.3428T=
XR_932837.1:n.3429T=
XR_932838.1:n.3429T=
NM_001351800.1:c.2851T= NP_001338729.1:p.Ser951=
NR_147784.1:n.3055T=
XM_011522479.2:c.3160T= XP_011520781.1:p.Ser1054=
XM_011522481.3:c.2851T= XP_011520783.1:p.Ser951=
XM_017023212.1:c.3025T= XP_016878701.1:p.Ser1009=
XM_017023214.1:c.3193T= XP_016878703.1:p.Ser1065=
XM_024450261.1:c.3229T= XP_024306029.1:p.Ser1077=
XR_932836.2:n.3374T=
XR_932837.3:n.3374T=
XR_932838.3:n.3374T=
NM_001171.6:c.3193T= MANE Select NP_001162.5:p.Ser1065=