Canonical Allele Identifier: CA2806037025

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16159464C>G , CM000678.2:g.16159464C>G	GRCh38
NC_000016.9:g.16253321C>G , CM000678.1:g.16253321C>G	GRCh37
NC_000016.8:g.16160822C>G	NCBI36
NG_007558.2:g.69008G>C
NG_007558.3:g.69154G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000622290.5:c.3735+18G>C	ENSP00000483331.2:n.3735+18G>C
ENST00000205557.12:c.3735+18G>C MANE Select	ENSP00000205557.7:n.3735+18G>C
ENST00000640696.1:c.549+18G>C	ENSP00000492197.1:n.549+18G>C
ENST00000205557.11:c.3735+18G>C	ENSP00000205557.7:n.3735+18G>C
ENST00000456970.6:c.3360+18G>C	ENSP00000405002.2:n.3360+18G>C
ENST00000622290.4:c.*944+18G>C	ENSP00000483331.1:n.*944+18G>C
NM_001171.5:c.3735+18G>C	NP_001162.4:n.3735+18G>C
XM_011522479.1:c.3702+18G>C	XP_011520781.1:n.3702+18G>C
XM_011522480.1:c.3393+18G>C	XP_011520782.1:n.3393+18G>C
XM_011522481.1:c.3393+18G>C	XP_011520783.1:n.3393+18G>C
XR_932836.1:n.3970+18G>C
XR_932837.1:n.3771+18G>C
XR_932838.1:n.3771+18G>C
XR_933134.1:n.539-317C>G
NM_001351800.1:c.3393+18G>C	NP_001338729.1:n.3393+18G>C
NR_147784.1:n.3397+18G>C
XM_011522479.2:c.3702+18G>C	XP_011520781.1:n.3702+18G>C
XM_011522481.3:c.3393+18G>C	XP_011520783.1:n.3393+18G>C
XM_017023212.1:c.3567+18G>C	XP_016878701.1:n.3567+18G>C
XM_024450261.1:c.3771+18G>C	XP_024306029.1:n.3771+18G>C
XR_932836.2:n.3916+18G>C
XR_932837.3:n.3716+18G>C
XR_932838.3:n.3716+18G>C
NM_001171.6:c.3735+18G>C MANE Select	NP_001162.5:n.3735+18G>C