Canonical Allele Identifier: CA2210135553

Gene: ABCC6

Linked Data

• dbSNP Id: rs749477982
• gnomAD v4: 16-16150830-TGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150832_16150833del , CM000678.2:g.16150832_16150833del	GRCh38
NC_000016.9:g.16244689_16244690del , CM000678.1:g.16244689_16244690del	GRCh37
NC_000016.8:g.16152190_16152191del	NCBI36
NG_007558.2:g.77640_77641del
NG_007558.3:g.77786_77787del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*381-60_*381-59del	ENSP00000483331.2:n.*381-60_*381-59del
ENST00000205557.12:c.4209-60_4209-59del MANE Select	ENSP00000205557.7:n.4209-60_4209-59del
ENST00000640696.1:c.1023-60_1023-59del	ENSP00000492197.1:n.1023-60_1023-59del
ENST00000205557.11:c.4209-60_4209-59del	ENSP00000205557.7:n.4209-60_4209-59del
ENST00000456970.6:c.3834-60_3834-59del	ENSP00000405002.2:n.3834-60_3834-59del
ENST00000576204.5:n.1072-60_1072-59del
ENST00000622290.4:c.*1418-60_*1418-59del	ENSP00000483331.1:n.*1418-60_*1418-59del
NM_001171.5:c.4209-60_4209-59del	NP_001162.4:n.4209-60_4209-59del
XM_011522479.1:c.4176-60_4176-59del	XP_011520781.1:n.4176-60_4176-59del
XM_011522480.1:c.3867-60_3867-59del	XP_011520782.1:n.3867-60_3867-59del
XM_011522481.1:c.3867-60_3867-59del	XP_011520783.1:n.3867-60_3867-59del
XR_933134.1:n.538+6542_538+6543del
NM_001351800.1:c.3867-60_3867-59del	NP_001338729.1:n.3867-60_3867-59del
NR_147784.1:n.3871-60_3871-59del
XM_011522479.2:c.4176-60_4176-59del	XP_011520781.1:n.4176-60_4176-59del
XM_011522481.3:c.3867-60_3867-59del	XP_011520783.1:n.3867-60_3867-59del
XM_017023212.1:c.4041-60_4041-59del	XP_016878701.1:n.4041-60_4041-59del
XM_024450261.1:c.4245-60_4245-59del	XP_024306029.1:n.4245-60_4245-59del
NM_001171.6:c.4209-60_4209-59del MANE Select	NP_001162.5:n.4209-60_4209-59del