Canonical Allele Identifier: CA3937918

Gene: ASCC3

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.100606829C>T , CM000668.2:g.100606829C>T	GRCh38
NC_000006.11:g.101054705C>T , CM000668.1:g.101054705C>T	GRCh37
NC_000006.10:g.101161426C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_006828.4:c.4955G>A MANE Select	NP_006819.2:p.Gly1652Asp
ENST00000369162.7:c.4955G>A MANE Select	ENSP00000358159.2:p.Gly1652Asp
NM_006828.3:c.4955G>A	NP_006819.2:p.Gly1652Asp
ENST00000369162.6:c.4955G>A	ENSP00000358159.2:p.Gly1652Asp
XM_011535394.1:c.4970G>A	XP_011533696.1:p.Gly1657Asp
XM_011535394.3:c.4970G>A	XP_011533696.1:p.Gly1657Asp
XM_011535395.1:c.4661G>A	XP_011533697.1:p.Gly1554Asp
XM_011535395.3:c.4661G>A	XP_011533697.1:p.Gly1554Asp
XM_011535396.1:c.4661G>A	XP_011533698.1:p.Gly1554Asp
XM_011535396.3:c.4661G>A	XP_011533698.1:p.Gly1554Asp
XM_017010205.2:c.4661G>A	XP_016865694.1:p.Gly1554Asp
XM_017010206.2:c.3536G>A	XP_016865695.1:p.Gly1179Asp
XM_024446316.1:c.4157G>A	XP_024302084.1:p.Gly1386Asp