Canonical Allele Identifier: CA2631961729

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16150109-TGGGGTAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150112_16150118del , CM000678.2:g.16150112_16150118del	GRCh38
NC_000016.9:g.16243969_16243975del , CM000678.1:g.16243969_16243975del	GRCh37
NC_000016.8:g.16151470_16151476del	NCBI36
NG_007558.2:g.78356_78362del
NG_007558.3:g.78502_78508del

Transcript Alleles

HGVS	Amino-acid change
ENST00000622290.5:c.*701_*707del	ENSP00000483331.2:n.*701_*707del
ENST00000205557.12:c.*17_*23del MANE Select	ENSP00000205557.7:n.*17_*23del
ENST00000640696.1:c.1343_1349del	ENSP00000492197.1:n.1343_1349del
ENST00000205557.11:c.*17_*23del	ENSP00000205557.7:n.*17_*23del
ENST00000576204.5:n.1392_1398del
ENST00000622290.4:c.*1738_*1744del	ENSP00000483331.1:n.*1738_*1744del
NM_001171.5:c.*17_*23del	NP_001162.4:n.*17_*23del
XM_011522479.1:c.*17_*23del	XP_011520781.1:n.*17_*23del
XM_011522480.1:c.*17_*23del	XP_011520782.1:n.*17_*23del
XM_011522481.1:c.*17_*23del	XP_011520783.1:n.*17_*23del
XR_933134.1:n.538+5822_538+5828del
NM_001351800.1:c.*17_*23del	NP_001338729.1:n.*17_*23del
NR_147784.1:n.4191_4197del
XM_011522479.2:c.*17_*23del	XP_011520781.1:n.*17_*23del
XM_011522481.3:c.*17_*23del	XP_011520783.1:n.*17_*23del
XM_017023212.1:c.*17_*23del	XP_016878701.1:n.*17_*23del
XM_024450261.1:c.*17_*23del	XP_024306029.1:n.*17_*23del
NM_001171.6:c.*17_*23del MANE Select	NP_001162.5:n.*17_*23del