Canonical Allele Identifier: CA2210139922
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16165725C= , CM000678.2:g.16165725C= GRCh38
NC_000016.9:g.16259582C= , CM000678.1:g.16259582C= GRCh37
NC_000016.8:g.16167083C= NCBI36
NG_007558.2:g.62747G=
NG_007558.3:g.62893G=

Transcript Alleles

HGVS Amino-acid change
ENST00000622290.5:c.3204G= ENSP00000483331.2:p.Met1068=
ENST00000205557.12:c.3204G= MANE Select ENSP00000205557.7:p.Met1068=
ENST00000640696.1:c.219G= ENSP00000492197.1:p.Met73=
ENST00000205557.11:c.3204G= ENSP00000205557.7:p.Met1068=
ENST00000456970.6:c.3029G= ENSP00000405002.2:n.3029G=
ENST00000622290.4:c.*413G= ENSP00000483331.1:n.*413G=
NM_001171.5:c.3204G= NP_001162.4:p.Met1068=
XM_011522479.1:c.3171G= XP_011520781.1:p.Met1057=
XM_011522480.1:c.2862G= XP_011520782.1:p.Met954=
XM_011522481.1:c.2862G= XP_011520783.1:p.Met954=
XR_932836.1:n.3439G=
XR_932837.1:n.3440G=
XR_932838.1:n.3440G=
NM_001351800.1:c.2862G= NP_001338729.1:p.Met954=
NR_147784.1:n.3066G=
XM_011522479.2:c.3171G= XP_011520781.1:p.Met1057=
XM_011522481.3:c.2862G= XP_011520783.1:p.Met954=
XM_017023212.1:c.3036G= XP_016878701.1:p.Met1012=
XM_017023214.1:c.3204G= XP_016878703.1:p.Met1068=
XM_024450261.1:c.3240G= XP_024306029.1:p.Met1080=
XR_932836.2:n.3385G=
XR_932837.3:n.3385G=
XR_932838.3:n.3385G=
NM_001171.6:c.3204G= MANE Select NP_001162.5:p.Met1068=