Canonical Allele Identifier: CA1682340065

Gene: C7orf50

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1044147_1044155delinsGCAGGTGTA , CM000669.2:g.1044147_1044155delinsGCAGGTGTA	GRCh38
NC_000007.13:g.1083783_1083791delinsGCAGGTGTA , CM000669.1:g.1083783_1083791delinsGCAGGTGTA	GRCh37
NC_000007.12:g.1050309_1050317delinsGCAGGTGTA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397098.8:c.130-34012_130-34004delinsTACACCTGC MANE Select	ENSP00000380286.3:n.130-34012_130-34004delinsTACACCTGC
ENST00000357429.10:c.130-34012_130-34004delinsTACACCTGC	ENSP00000350011.5:n.130-34012_130-34004delinsTACACCTGC
ENST00000397098.7:c.130-34012_130-34004delinsTACACCTGC	ENSP00000380286.3:n.130-34012_130-34004delinsTACACCTGC
ENST00000397100.6:c.130-34012_130-34004delinsTACACCTGC	ENSP00000380288.2:n.130-34012_130-34004delinsTACACCTGC
ENST00000444428.5:c.33+11119_33+11127delinsTACACCTGC	ENSP00000396542.1:n.33+11119_33+11127delinsTACACCTGC
ENST00000488073.1:n.267-34012_267-34004delinsTACACCTGC
ENST00000491163.1:c.130-34012_130-34004delinsTACACCTGC	ENSP00000420130.1:n.130-34012_130-34004delinsTACACCTGC
NM_001134395.1:c.130-34012_130-34004delinsTACACCTGC	NP_001127867.1:n.130-34012_130-34004delinsTACACCTGC
NM_001134396.1:c.130-34012_130-34004delinsTACACCTGC	NP_001127868.1:n.130-34012_130-34004delinsTACACCTGC
NM_032350.5:c.130-34012_130-34004delinsTACACCTGC	NP_115726.1:n.130-34012_130-34004delinsTACACCTGC
XM_005249888.3:c.130-34012_130-34004delinsTACACCTGC	XP_005249945.1:n.130-34012_130-34004delinsTACACCTGC
XM_011515581.1:c.130-34012_130-34004delinsTACACCTGC	XP_011513883.1:n.130-34012_130-34004delinsTACACCTGC
XM_011515582.1:c.130-34012_130-34004delinsTACACCTGC	XP_011513884.1:n.130-34012_130-34004delinsTACACCTGC
XM_011515583.1:c.130-34012_130-34004delinsTACACCTGC	XP_011513885.1:n.130-34012_130-34004delinsTACACCTGC
XM_011515584.1:c.130-34012_130-34004delinsTACACCTGC	XP_011513886.1:n.130-34012_130-34004delinsTACACCTGC
NM_001318252.1:c.130-34012_130-34004delinsTACACCTGC	NP_001305181.1:n.130-34012_130-34004delinsTACACCTGC
NM_001350968.1:c.130-34012_130-34004delinsTACACCTGC	NP_001337897.1:n.130-34012_130-34004delinsTACACCTGC
XM_011515581.3:c.130-34012_130-34004delinsTACACCTGC	XP_011513883.1:n.130-34012_130-34004delinsTACACCTGC
XM_011515582.3:c.130-34012_130-34004delinsTACACCTGC	XP_011513884.1:n.130-34012_130-34004delinsTACACCTGC
XM_011515583.2:c.130-34012_130-34004delinsTACACCTGC	XP_011513885.1:n.130-34012_130-34004delinsTACACCTGC
XM_011515584.2:c.130-34012_130-34004delinsTACACCTGC	XP_011513886.1:n.130-34012_130-34004delinsTACACCTGC
XM_017012720.2:c.130-34012_130-34004delinsTACACCTGC	XP_016868209.1:n.130-34012_130-34004delinsTACACCTGC
XM_017012721.2:c.-144-22564_-144-22556delinsTACACCTGC	XP_016868210.1:n.-144-22564_-144-22556delinsTACACCTGC
XM_024446977.1:c.130-34012_130-34004delinsTACACCTGC	XP_024302745.1:n.130-34012_130-34004delinsTACACCTGC
XM_024446978.1:c.-144-22564_-144-22556delinsTACACCTGC	XP_024302746.1:n.-144-22564_-144-22556delinsTACACCTGC
NM_001318252.2:c.130-34012_130-34004delinsTACACCTGC MANE Select	NP_001305181.1:n.130-34012_130-34004delinsTACACCTGC