Canonical Allele Identifier: CA2806039941

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16169891_16169892insAG , CM000678.2:g.16169891_16169892insAG	GRCh38
NC_000016.9:g.16263748_16263749insAG , CM000678.1:g.16263748_16263749insAG	GRCh37
NC_000016.8:g.16171249_16171250insAG	NCBI36
NG_007558.2:g.58580_58581insCT
NG_007558.3:g.58726_58727insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.2788-39_2788-38insCT	ENSP00000483331.2:n.2788-39_2788-38insCT
ENST00000205557.12:c.2788-39_2788-38insCT MANE Select	ENSP00000205557.7:n.2788-39_2788-38insCT
ENST00000205557.11:c.2788-39_2788-38insCT	ENSP00000205557.7:n.2788-39_2788-38insCT
ENST00000456970.6:c.2613-39_2613-38insCT	ENSP00000405002.2:n.2613-39_2613-38insCT
ENST00000622290.4:c.2613-39_2613-38insCT	ENSP00000483331.1:n.2613-39_2613-38insCT
NM_001171.5:c.2788-39_2788-38insCT	NP_001162.4:n.2788-39_2788-38insCT
XM_011522479.1:c.2755-39_2755-38insCT	XP_011520781.1:n.2755-39_2755-38insCT
XM_011522480.1:c.2446-39_2446-38insCT	XP_011520782.1:n.2446-39_2446-38insCT
XM_011522481.1:c.2446-39_2446-38insCT	XP_011520783.1:n.2446-39_2446-38insCT
XR_932836.1:n.3023-39_3023-38insCT
XR_932837.1:n.3024-39_3024-38insCT
XR_932838.1:n.3024-39_3024-38insCT
NM_001351800.1:c.2446-39_2446-38insCT	NP_001338729.1:n.2446-39_2446-38insCT
NR_147784.1:n.2650-39_2650-38insCT
XM_011522479.2:c.2755-39_2755-38insCT	XP_011520781.1:n.2755-39_2755-38insCT
XM_011522481.3:c.2446-39_2446-38insCT	XP_011520783.1:n.2446-39_2446-38insCT
XM_017023212.1:c.2620-39_2620-38insCT	XP_016878701.1:n.2620-39_2620-38insCT
XM_017023214.1:c.2788-39_2788-38insCT	XP_016878703.1:n.2788-39_2788-38insCT
XM_024450261.1:c.2824-39_2824-38insCT	XP_024306029.1:n.2824-39_2824-38insCT
XR_932836.2:n.2969-39_2969-38insCT
XR_932837.3:n.2969-39_2969-38insCT
XR_932838.3:n.2969-39_2969-38insCT
NM_001171.6:c.2788-39_2788-38insCT MANE Select	NP_001162.5:n.2788-39_2788-38insCT