Canonical Allele Identifier: CA2806037762

Gene: ABCC6

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.16162964A>G , CM000678.2:g.16162964A>G	GRCh38
NC_000016.9:g.16256821A>G , CM000678.1:g.16256821A>G	GRCh37
NC_000016.8:g.16164322A>G	NCBI36
NG_007558.2:g.65508T>C
NG_007558.3:g.65654T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000622290.5:c.3506+29T>C	ENSP00000483331.2:n.3506+29T>C
ENST00000205557.12:c.3506+29T>C MANE Select	ENSP00000205557.7:n.3506+29T>C
ENST00000640696.1:c.321-1400T>C	ENSP00000492197.1:n.321-1400T>C
ENST00000205557.11:c.3506+29T>C	ENSP00000205557.7:n.3506+29T>C
ENST00000456970.6:c.3132-1400T>C	ENSP00000405002.2:n.3132-1400T>C
ENST00000622290.4:c.*715+29T>C	ENSP00000483331.1:n.*715+29T>C
NM_001171.5:c.3506+29T>C	NP_001162.4:n.3506+29T>C
XM_011522479.1:c.3473+29T>C	XP_011520781.1:n.3473+29T>C
XM_011522480.1:c.3164+29T>C	XP_011520782.1:n.3164+29T>C
XM_011522481.1:c.3164+29T>C	XP_011520783.1:n.3164+29T>C
XR_932836.1:n.3741+29T>C
XR_932837.1:n.3543-1400T>C
XR_932838.1:n.3543-1400T>C
XR_933133.1:n.407+121A>G
XR_933134.1:n.754+121A>G
NM_001351800.1:c.3164+29T>C	NP_001338729.1:n.3164+29T>C
NR_147784.1:n.3169-1400T>C
XM_011522479.2:c.3473+29T>C	XP_011520781.1:n.3473+29T>C
XM_011522481.3:c.3164+29T>C	XP_011520783.1:n.3164+29T>C
XM_017023212.1:c.3338+29T>C	XP_016878701.1:n.3338+29T>C
XM_017023214.1:c.3307-1400T>C	XP_016878703.1:n.3307-1400T>C
XM_024450261.1:c.3542+29T>C	XP_024306029.1:n.3542+29T>C
XR_932836.2:n.3687+29T>C
XR_932837.3:n.3488-1400T>C
XR_932838.3:n.3488-1400T>C
NM_001171.6:c.3506+29T>C MANE Select	NP_001162.5:n.3506+29T>C