Canonical Allele Identifier: CA2210143343
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16169864_16169866delinsCAT , CM000678.2:g.16169864_16169866delinsCAT GRCh38
NC_000016.9:g.16263721_16263723delinsCAT , CM000678.1:g.16263721_16263723delinsCAT GRCh37
NC_000016.8:g.16171222_16171224delinsCAT NCBI36
NG_007558.2:g.58606_58608delinsATG
NG_007558.3:g.58752_58754delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000622290.5:c.2788-13_2788-11delinsATG ENSP00000483331.2:n.2788-13_2788-11delinsATG
ENST00000205557.12:c.2788-13_2788-11delinsATG MANE Select ENSP00000205557.7:n.2788-13_2788-11delinsATG
ENST00000205557.11:c.2788-13_2788-11delinsATG ENSP00000205557.7:n.2788-13_2788-11delinsATG
ENST00000456970.6:c.2613-13_2613-11delinsATG ENSP00000405002.2:n.2613-13_2613-11delinsATG
ENST00000622290.4:c.2613-13_2613-11delinsATG ENSP00000483331.1:n.2613-13_2613-11delinsATG
NM_001171.5:c.2788-13_2788-11delinsATG NP_001162.4:n.2788-13_2788-11delinsATG
XM_011522479.1:c.2755-13_2755-11delinsATG XP_011520781.1:n.2755-13_2755-11delinsATG
XM_011522480.1:c.2446-13_2446-11delinsATG XP_011520782.1:n.2446-13_2446-11delinsATG
XM_011522481.1:c.2446-13_2446-11delinsATG XP_011520783.1:n.2446-13_2446-11delinsATG
XR_932836.1:n.3023-13_3023-11delinsATG
XR_932837.1:n.3024-13_3024-11delinsATG
XR_932838.1:n.3024-13_3024-11delinsATG
NM_001351800.1:c.2446-13_2446-11delinsATG NP_001338729.1:n.2446-13_2446-11delinsATG
NR_147784.1:n.2650-13_2650-11delinsATG
XM_011522479.2:c.2755-13_2755-11delinsATG XP_011520781.1:n.2755-13_2755-11delinsATG
XM_011522481.3:c.2446-13_2446-11delinsATG XP_011520783.1:n.2446-13_2446-11delinsATG
XM_017023212.1:c.2620-13_2620-11delinsATG XP_016878701.1:n.2620-13_2620-11delinsATG
XM_017023214.1:c.2788-13_2788-11delinsATG XP_016878703.1:n.2788-13_2788-11delinsATG
XM_024450261.1:c.2824-13_2824-11delinsATG XP_024306029.1:n.2824-13_2824-11delinsATG
XR_932836.2:n.2969-13_2969-11delinsATG
XR_932837.3:n.2969-13_2969-11delinsATG
XR_932838.3:n.2969-13_2969-11delinsATG
NM_001171.6:c.2788-13_2788-11delinsATG MANE Select NP_001162.5:n.2788-13_2788-11delinsATG