Canonical Allele Identifier: CA365124921

Gene: ASCC3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.100540245T>C , CM000668.2:g.100540245T>C	GRCh38
NC_000006.11:g.100988121T>C , CM000668.1:g.100988121T>C	GRCh37
NC_000006.10:g.101094842T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006828.4:c.5693A>G MANE Select	NP_006819.2:p.His1898Arg
ENST00000369162.7:c.5693A>G MANE Select	ENSP00000358159.2:p.His1898Arg
NM_006828.3:c.5693A>G	NP_006819.2:p.His1898Arg
ENST00000369162.6:c.5693A>G	ENSP00000358159.2:p.His1898Arg
XM_011535394.1:c.5708A>G	XP_011533696.1:p.His1903Arg
XM_011535394.3:c.5708A>G	XP_011533696.1:p.His1903Arg
XM_011535395.1:c.5399A>G	XP_011533697.1:p.His1800Arg
XM_011535395.3:c.5399A>G	XP_011533697.1:p.His1800Arg
XM_011535396.1:c.5399A>G	XP_011533698.1:p.His1800Arg
XM_011535396.3:c.5399A>G	XP_011533698.1:p.His1800Arg
XM_017010205.2:c.5399A>G	XP_016865694.1:p.His1800Arg
XM_017010206.2:c.4274A>G	XP_016865695.1:p.His1425Arg
XM_024446316.1:c.4895A>G	XP_024302084.1:p.His1632Arg