Canonical Allele Identifier: CA2806037434

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16150875_16150876insAGA , CM000678.2:g.16150875_16150876insAGA	GRCh38
NC_000016.9:g.16244732_16244733insAGA , CM000678.1:g.16244732_16244733insAGA	GRCh37
NC_000016.8:g.16152233_16152234insAGA	NCBI36
NG_007558.2:g.77596_77597insTCT
NG_007558.3:g.77742_77743insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.*381-104_*381-103insTCT	ENSP00000483331.2:n.*381-104_*381-103insTCT
ENST00000205557.12:c.4209-104_4209-103insTCT MANE Select	ENSP00000205557.7:n.4209-104_4209-103insTCT
ENST00000640696.1:c.1023-104_1023-103insTCT	ENSP00000492197.1:n.1023-104_1023-103insTCT
ENST00000205557.11:c.4209-104_4209-103insTCT	ENSP00000205557.7:n.4209-104_4209-103insTCT
ENST00000456970.6:c.3834-104_3834-103insTCT	ENSP00000405002.2:n.3834-104_3834-103insTCT
ENST00000576204.5:n.1072-104_1072-103insTCT
ENST00000622290.4:c.*1418-104_*1418-103insTCT	ENSP00000483331.1:n.*1418-104_*1418-103insTCT
NM_001171.5:c.4209-104_4209-103insTCT	NP_001162.4:n.4209-104_4209-103insTCT
XM_011522479.1:c.4176-104_4176-103insTCT	XP_011520781.1:n.4176-104_4176-103insTCT
XM_011522480.1:c.3867-104_3867-103insTCT	XP_011520782.1:n.3867-104_3867-103insTCT
XM_011522481.1:c.3867-104_3867-103insTCT	XP_011520783.1:n.3867-104_3867-103insTCT
XR_933134.1:n.538+6585_538+6586insAGA
NM_001351800.1:c.3867-104_3867-103insTCT	NP_001338729.1:n.3867-104_3867-103insTCT
NR_147784.1:n.3871-104_3871-103insTCT
XM_011522479.2:c.4176-104_4176-103insTCT	XP_011520781.1:n.4176-104_4176-103insTCT
XM_011522481.3:c.3867-104_3867-103insTCT	XP_011520783.1:n.3867-104_3867-103insTCT
XM_017023212.1:c.4041-104_4041-103insTCT	XP_016878701.1:n.4041-104_4041-103insTCT
XM_024450261.1:c.4245-104_4245-103insTCT	XP_024306029.1:n.4245-104_4245-103insTCT
NM_001171.6:c.4209-104_4209-103insTCT MANE Select	NP_001162.5:n.4209-104_4209-103insTCT