Canonical Allele Identifier: CA2806037999
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155147_16155148insAC , CM000678.2:g.16155147_16155148insAC GRCh38
NC_000016.9:g.16249004_16249005insAC , CM000678.1:g.16249004_16249005insAC GRCh37
NC_000016.8:g.16156505_16156506insAC NCBI36
NG_007558.2:g.73325_73326insTG
NG_007558.3:g.73471_73472insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.630_631insTG
ENST00000622290.5:c.*55-116_*55-115insTG ENSP00000483331.2:n.*55-116_*55-115insTG
ENST00000205557.12:c.3883-116_3883-115insTG MANE Select ENSP00000205557.7:n.3883-116_3883-115insTG
ENST00000640696.1:c.697-116_697-115insTG ENSP00000492197.1:n.697-116_697-115insTG
ENST00000205557.11:c.3883-116_3883-115insTG ENSP00000205557.7:n.3883-116_3883-115insTG
ENST00000456970.6:c.3508-116_3508-115insTG ENSP00000405002.2:n.3508-116_3508-115insTG
ENST00000576204.5:n.630_631insTG
ENST00000622290.4:c.*1092-116_*1092-115insTG ENSP00000483331.1:n.*1092-116_*1092-115insTG
NM_001171.5:c.3883-116_3883-115insTG NP_001162.4:n.3883-116_3883-115insTG
XM_011522479.1:c.3850-116_3850-115insTG XP_011520781.1:n.3850-116_3850-115insTG
XM_011522480.1:c.3541-116_3541-115insTG XP_011520782.1:n.3541-116_3541-115insTG
XM_011522481.1:c.3541-116_3541-115insTG XP_011520783.1:n.3541-116_3541-115insTG
XR_932836.1:n.4181-116_4181-115insTG
XR_932837.1:n.3919-116_3919-115insTG
XR_932838.1:n.3982-116_3982-115insTG
XR_933134.1:n.539-4634_539-4633insAC
NM_001351800.1:c.3541-116_3541-115insTG NP_001338729.1:n.3541-116_3541-115insTG
NR_147784.1:n.3545-116_3545-115insTG
XM_011522479.2:c.3850-116_3850-115insTG XP_011520781.1:n.3850-116_3850-115insTG
XM_011522481.3:c.3541-116_3541-115insTG XP_011520783.1:n.3541-116_3541-115insTG
XM_017023212.1:c.3715-116_3715-115insTG XP_016878701.1:n.3715-116_3715-115insTG
XM_024450261.1:c.3919-116_3919-115insTG XP_024306029.1:n.3919-116_3919-115insTG
XR_932836.2:n.4127-116_4127-115insTG
XR_932837.3:n.3864-116_3864-115insTG
XR_932838.3:n.3927-116_3927-115insTG
NM_001171.6:c.3883-116_3883-115insTG MANE Select NP_001162.5:n.3883-116_3883-115insTG