Canonical Allele Identifier: CA2832584435

Gene: CBX7

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.39146287G>C , CM000684.2:g.39146287G>C	GRCh38
NC_000022.10:g.39542292G>C , CM000684.1:g.39542292G>C	GRCh37
NC_000022.9:g.37872238G>C	NCBI36
NG_051974.1:g.11364C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_175709.5:c.113+3502C>G MANE Select	NP_783640.1:n.113+3502C>G
ENST00000216133.10:c.113+3502C>G MANE Select	ENSP00000216133.5:n.113+3502C>G
NM_001346743.1:c.113+3502C>G	NP_001333672.1:n.113+3502C>G
NM_001346743.2:c.113+3502C>G	NP_001333672.1:n.113+3502C>G
NM_001346744.1:c.113+3502C>G	NP_001333673.1:n.113+3502C>G
NM_001346744.2:c.113+3502C>G	NP_001333673.1:n.113+3502C>G
NM_175709.3:c.113+3502C>G	NP_783640.1:n.113+3502C>G
NM_175709.4:c.113+3502C>G	NP_783640.1:n.113+3502C>G
ENST00000216133.9:c.113+3502C>G	ENSP00000216133.5:n.113+3502C>G
ENST00000401405.7:c.113+3502C>G	ENSP00000384035.3:n.113+3502C>G
ENST00000434260.1:c.113+3502C>G	ENSP00000410896.1:n.113+3502C>G
ENST00000475962.5:n.44+3502C>G
ENST00000477827.1:n.209+3502C>G
XM_005261413.3:c.113+3502C>G	XP_005261470.1:n.113+3502C>G
XM_006724174.2:c.113+3502C>G	XP_006724237.1:n.113+3502C>G
XM_006724174.4:c.113+3502C>G	XP_006724237.1:n.113+3502C>G
XM_006724175.2:c.113+3502C>G	XP_006724238.1:n.113+3502C>G
XM_006724175.4:c.113+3502C>G	XP_006724238.1:n.113+3502C>G
XM_006724176.2:c.113+3502C>G	XP_006724239.1:n.113+3502C>G
XM_006724176.4:c.113+3502C>G	XP_006724239.1:n.113+3502C>G
XM_006724177.2:c.113+3502C>G	XP_006724240.1:n.113+3502C>G
XM_006724177.4:c.113+3502C>G	XP_006724240.1:n.113+3502C>G
XM_006724178.2:c.113+3502C>G	XP_006724241.1:n.113+3502C>G
XM_006724178.4:c.113+3502C>G	XP_006724241.1:n.113+3502C>G
XM_011530025.1:c.113+3502C>G	XP_011528327.1:n.113+3502C>G
XM_011530025.3:c.113+3502C>G	XP_011528327.1:n.113+3502C>G