Canonical Allele Identifier: CA2631963755

Gene: ABCC6

Linked Data

• gnomAD v4: 16-16150880-GTGTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150881_16150884del , CM000678.2:g.16150881_16150884del	GRCh38
NC_000016.9:g.16244738_16244741del , CM000678.1:g.16244738_16244741del	GRCh37
NC_000016.8:g.16152239_16152242del	NCBI36
NG_007558.2:g.77588_77591del
NG_007558.3:g.77734_77737del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*381-112_*381-109del	ENSP00000483331.2:n.*381-112_*381-109del
ENST00000205557.12:c.4209-112_4209-109del MANE Select	ENSP00000205557.7:n.4209-112_4209-109del
ENST00000640696.1:c.1023-112_1023-109del	ENSP00000492197.1:n.1023-112_1023-109del
ENST00000205557.11:c.4209-112_4209-109del	ENSP00000205557.7:n.4209-112_4209-109del
ENST00000456970.6:c.3834-112_3834-109del	ENSP00000405002.2:n.3834-112_3834-109del
ENST00000576204.5:n.1072-112_1072-109del
ENST00000622290.4:c.*1418-112_*1418-109del	ENSP00000483331.1:n.*1418-112_*1418-109del
NM_001171.5:c.4209-112_4209-109del	NP_001162.4:n.4209-112_4209-109del
XM_011522479.1:c.4176-112_4176-109del	XP_011520781.1:n.4176-112_4176-109del
XM_011522480.1:c.3867-112_3867-109del	XP_011520782.1:n.3867-112_3867-109del
XM_011522481.1:c.3867-112_3867-109del	XP_011520783.1:n.3867-112_3867-109del
XR_933134.1:n.538+6591_538+6594del
NM_001351800.1:c.3867-112_3867-109del	NP_001338729.1:n.3867-112_3867-109del
NR_147784.1:n.3871-112_3871-109del
XM_011522479.2:c.4176-112_4176-109del	XP_011520781.1:n.4176-112_4176-109del
XM_011522481.3:c.3867-112_3867-109del	XP_011520783.1:n.3867-112_3867-109del
XM_017023212.1:c.4041-112_4041-109del	XP_016878701.1:n.4041-112_4041-109del
XM_024450261.1:c.4245-112_4245-109del	XP_024306029.1:n.4245-112_4245-109del
NM_001171.6:c.4209-112_4209-109del MANE Select	NP_001162.5:n.4209-112_4209-109del