Canonical Allele Identifier: CA2631961203

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16149826-T-TTACC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16149826_16149827insTACC , CM000678.2:g.16149826_16149827insTACC	GRCh38
NC_000016.9:g.16243683_16243684insTACC , CM000678.1:g.16243683_16243684insTACC	GRCh37
NC_000016.8:g.16151184_16151185insTACC	NCBI36
NG_007558.2:g.78645_78646insGGTA
NG_007558.3:g.78791_78792insGGTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*990_*991insGGTA	ENSP00000483331.2:n.*990_*991insGGTA
ENST00000205557.12:c.*306_*307insGGTA MANE Select	ENSP00000205557.7:n.*306_*307insGGTA
ENST00000640696.1:c.1632_1633insGGTA	ENSP00000492197.1:n.1632_1633insGGTA
ENST00000205557.11:c.*306_*307insGGTA	ENSP00000205557.7:n.*306_*307insGGTA
ENST00000576204.5:n.1681_1682insGGTA
ENST00000622290.4:c.*2027_*2028insGGTA	ENSP00000483331.1:n.*2027_*2028insGGTA
NM_001171.5:c.*306_*307insGGTA	NP_001162.4:n.*306_*307insGGTA
XM_011522479.1:c.*306_*307insGGTA	XP_011520781.1:n.*306_*307insGGTA
XM_011522480.1:c.*306_*307insGGTA	XP_011520782.1:n.*306_*307insGGTA
XM_011522481.1:c.*306_*307insGGTA	XP_011520783.1:n.*306_*307insGGTA
XR_933134.1:n.538+5536_538+5537insTACC
NM_001351800.1:c.*306_*307insGGTA	NP_001338729.1:n.*306_*307insGGTA
NR_147784.1:n.4480_4481insGGTA
XM_011522479.2:c.*306_*307insGGTA	XP_011520781.1:n.*306_*307insGGTA
XM_011522481.3:c.*306_*307insGGTA	XP_011520783.1:n.*306_*307insGGTA
XM_017023212.1:c.*306_*307insGGTA	XP_016878701.1:n.*306_*307insGGTA
XM_024450261.1:c.*306_*307insGGTA	XP_024306029.1:n.*306_*307insGGTA
NM_001171.6:c.*306_*307insGGTA MANE Select	NP_001162.5:n.*306_*307insGGTA