Canonical Allele Identifier: CA2806038405

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16198287_16198288insACA , CM000678.2:g.16198287_16198288insACA	GRCh38
NC_000016.9:g.16292144_16292145insACA , CM000678.1:g.16292144_16292145insACA	GRCh37
NC_000016.8:g.16199645_16199646insACA	NCBI36
NG_007558.2:g.30184_30185insTGT
NG_007558.3:g.30330_30331insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574094.6:c.1177-106_1177-105insTGT	ENSP00000507301.1:n.1177-106_1177-105insTGT
ENST00000622290.5:c.1177-106_1177-105insTGT	ENSP00000483331.2:n.1177-106_1177-105insTGT
ENST00000205557.12:c.1177-106_1177-105insTGT MANE Select	ENSP00000205557.7:n.1177-106_1177-105insTGT
ENST00000205557.11:c.1177-106_1177-105insTGT	ENSP00000205557.7:n.1177-106_1177-105insTGT
ENST00000456970.6:c.1177-106_1177-105insTGT	ENSP00000405002.2:n.1177-106_1177-105insTGT
ENST00000574094.5:n.1273-106_1273-105insTGT
ENST00000622290.4:c.1177-106_1177-105insTGT	ENSP00000483331.1:n.1177-106_1177-105insTGT
NM_001171.5:c.1177-106_1177-105insTGT	NP_001162.4:n.1177-106_1177-105insTGT
XM_011522479.1:c.1177-106_1177-105insTGT	XP_011520781.1:n.1177-106_1177-105insTGT
XM_011522480.1:c.835-106_835-105insTGT	XP_011520782.1:n.835-106_835-105insTGT
XM_011522481.1:c.835-106_835-105insTGT	XP_011520783.1:n.835-106_835-105insTGT
XM_011522482.1:c.1177-106_1177-105insTGT	XP_011520784.1:n.1177-106_1177-105insTGT
XR_932836.1:n.1412-106_1412-105insTGT
XR_932837.1:n.1413-106_1413-105insTGT
XR_932838.1:n.1413-106_1413-105insTGT
NM_001351800.1:c.835-106_835-105insTGT	NP_001338729.1:n.835-106_835-105insTGT
NR_147784.1:n.1214-106_1214-105insTGT
XM_011522479.2:c.1177-106_1177-105insTGT	XP_011520781.1:n.1177-106_1177-105insTGT
XM_011522481.3:c.835-106_835-105insTGT	XP_011520783.1:n.835-106_835-105insTGT
XM_011522482.3:c.1177-106_1177-105insTGT	XP_011520784.1:n.1177-106_1177-105insTGT
XM_017023212.1:c.1177-106_1177-105insTGT	XP_016878701.1:n.1177-106_1177-105insTGT
XM_017023214.1:c.1177-106_1177-105insTGT	XP_016878703.1:n.1177-106_1177-105insTGT
XM_024450261.1:c.1213-106_1213-105insTGT	XP_024306029.1:n.1213-106_1213-105insTGT
XR_932836.2:n.1358-106_1358-105insTGT
XR_932837.3:n.1358-106_1358-105insTGT
XR_932838.3:n.1358-106_1358-105insTGT
NM_001171.6:c.1177-106_1177-105insTGT MANE Select	NP_001162.5:n.1177-106_1177-105insTGT