Canonical Allele Identifier: CA813117286

Gene: ADAMTS6

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.65151950C>G , CM000667.2:g.65151950C>G	GRCh38
NC_000005.9:g.64447777C>G , CM000667.1:g.64447777C>G	GRCh37
NC_000005.8:g.64483533C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381055.8:c.3245-5G>C MANE Select	ENSP00000370443.3:n.3245-5G>C
ENST00000314351.9:n.905-5G>C
ENST00000381052.8:c.*2517-5G>C	ENSP00000424377.1:n.*2517-5G>C
ENST00000381055.7:c.3245-5G>C	ENSP00000370443.3:n.3245-5G>C
NM_197941.2:c.3245-5G>C	NP_922932.2:n.3245-5G>C
XM_011543113.1:c.3245-5G>C	XP_011541415.1:n.3245-5G>C
XM_011543114.1:c.3245-5G>C	XP_011541416.1:n.3245-5G>C
XM_011543115.1:c.3095-5G>C	XP_011541417.1:n.3095-5G>C
XM_011543116.1:c.2957-5G>C	XP_011541418.1:n.2957-5G>C
XM_011543117.1:c.2792-5G>C	XP_011541419.1:n.2792-5G>C
XM_011543121.1:c.2471-5G>C	XP_011541423.1:n.2471-5G>C
XM_011543123.1:c.2108-5G>C	XP_011541425.1:n.2108-5G>C
XM_011543124.1:c.1913-5G>C	XP_011541426.1:n.1913-5G>C
XM_011543125.1:c.1778-5G>C	XP_011541427.1:n.1778-5G>C
XR_948232.1:n.4289-5G>C
NM_197941.3:c.3245-5G>C	NP_922932.2:n.3245-5G>C
NR_135689.1:n.4253-5G>C
XM_011543113.3:c.3245-5G>C	XP_011541415.1:n.3245-5G>C
XM_011543114.3:c.3245-5G>C	XP_011541416.1:n.3245-5G>C
XM_011543115.3:c.3095-5G>C	XP_011541417.1:n.3095-5G>C
XM_011543116.3:c.2957-5G>C	XP_011541418.1:n.2957-5G>C
XM_011543117.2:c.2792-5G>C	XP_011541419.1:n.2792-5G>C
XM_011543121.2:c.2483-5G>C	XP_011541423.2:n.2483-5G>C
XM_011543123.2:c.2108-5G>C	XP_011541425.1:n.2108-5G>C
XM_011543124.2:c.1913-5G>C	XP_011541426.1:n.1913-5G>C
XR_948232.3:n.4244-5G>C
NM_197941.4:c.3245-5G>C MANE Select	NP_922932.2:n.3245-5G>C
NR_135689.2:n.4253-5G>C