Canonical Allele Identifier: CA2806038156
Gene: ABCC6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.16155345_16155346insAGT , CM000678.2:g.16155345_16155346insAGT GRCh38
NC_000016.9:g.16249202_16249203insAGT , CM000678.1:g.16249202_16249203insAGT GRCh37
NC_000016.8:g.16156703_16156704insAGT NCBI36
NG_007558.2:g.73127_73128insCTA
NG_007558.3:g.73273_73274insCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000576204.6:n.432_433insCTA
ENST00000622290.5:c.*55-314_*55-313insCTA ENSP00000483331.2:n.*55-314_*55-313insCTA
ENST00000205557.12:c.3883-314_3883-313insCTA MANE Select ENSP00000205557.7:n.3883-314_3883-313insCTA
ENST00000640696.1:c.697-314_697-313insCTA ENSP00000492197.1:n.697-314_697-313insCTA
ENST00000205557.11:c.3883-314_3883-313insCTA ENSP00000205557.7:n.3883-314_3883-313insCTA
ENST00000456970.6:c.3508-314_3508-313insCTA ENSP00000405002.2:n.3508-314_3508-313insCTA
ENST00000576204.5:n.432_433insCTA
ENST00000622290.4:c.*1092-314_*1092-313insCTA ENSP00000483331.1:n.*1092-314_*1092-313insCTA
NM_001171.5:c.3883-314_3883-313insCTA NP_001162.4:n.3883-314_3883-313insCTA
XM_011522479.1:c.3850-314_3850-313insCTA XP_011520781.1:n.3850-314_3850-313insCTA
XM_011522480.1:c.3541-314_3541-313insCTA XP_011520782.1:n.3541-314_3541-313insCTA
XM_011522481.1:c.3541-314_3541-313insCTA XP_011520783.1:n.3541-314_3541-313insCTA
XR_932836.1:n.4181-314_4181-313insCTA
XR_932837.1:n.3919-314_3919-313insCTA
XR_932838.1:n.3982-314_3982-313insCTA
XR_933134.1:n.539-4436_539-4435insAGT
NM_001351800.1:c.3541-314_3541-313insCTA NP_001338729.1:n.3541-314_3541-313insCTA
NR_147784.1:n.3545-314_3545-313insCTA
XM_011522479.2:c.3850-314_3850-313insCTA XP_011520781.1:n.3850-314_3850-313insCTA
XM_011522481.3:c.3541-314_3541-313insCTA XP_011520783.1:n.3541-314_3541-313insCTA
XM_017023212.1:c.3715-314_3715-313insCTA XP_016878701.1:n.3715-314_3715-313insCTA
XM_024450261.1:c.3919-314_3919-313insCTA XP_024306029.1:n.3919-314_3919-313insCTA
XR_932836.2:n.4127-314_4127-313insCTA
XR_932837.3:n.3864-314_3864-313insCTA
XR_932838.3:n.3927-314_3927-313insCTA
NM_001171.6:c.3883-314_3883-313insCTA MANE Select NP_001162.5:n.3883-314_3883-313insCTA