Canonical Allele Identifier: CA2830536676
Gene: FRYL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.48589966del , CM000666.2:g.48589966del GRCh38
NC_000004.11:g.48591983del , CM000666.1:g.48591983del GRCh37
NC_000004.10:g.48286740del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000507873.8:c.1508-89del ENSP00000422408.4:n.1508-89del
ENST00000358350.9:c.1508-89del MANE Select ENSP00000351113.4:n.1508-89del
ENST00000503238.6:c.1508-89del ENSP00000426064.2:n.1508-89del
ENST00000673760.1:c.1661-89del ENSP00000501160.1:n.1661-89del
ENST00000358350.8:c.1508-89del ENSP00000351113.4:n.1508-89del
ENST00000503238.5:c.1508-89del ENSP00000426064.1:n.1508-89del
ENST00000506685.1:c.626-89del ENSP00000425592.1:n.626-89del
ENST00000507711.5:c.1508-89del ENSP00000421584.1:n.1508-89del
NM_015030.1:c.1508-89del NP_055845.1:n.1508-89del
XM_005248090.3:c.1553-89del XP_005248147.1:n.1553-89del
XM_011513680.1:c.1553-89del XP_011511982.1:n.1553-89del
XM_011513681.1:c.1553-89del XP_011511983.1:n.1553-89del
XM_011513682.1:c.1508-89del XP_011511984.1:n.1508-89del
XM_011513683.1:c.1553-89del XP_011511985.1:n.1553-89del
XM_011513685.1:c.1553-89del XP_011511987.1:n.1553-89del
XR_925126.1:n.1633-89del
XM_005248090.5:c.1553-89del XP_005248147.1:n.1553-89del
XM_011513680.3:c.1829-89del XP_011511982.2:n.1829-89del
XM_011513681.3:c.1829-89del XP_011511983.2:n.1829-89del
XM_011513682.3:c.1784-89del XP_011511984.2:n.1784-89del
XM_011513683.3:c.1553-89del XP_011511985.1:n.1553-89del
XM_011513685.3:c.1829-89del XP_011511987.2:n.1829-89del
XM_017008046.2:c.1508-89del XP_016863535.1:n.1508-89del
XM_024453988.1:c.1829-89del XP_024309756.1:n.1829-89del
XM_024453989.1:c.1784-89del XP_024309757.1:n.1784-89del
XM_024453990.1:c.1553-89del XP_024309758.1:n.1553-89del
XM_024453991.1:c.1553-89del XP_024309759.1:n.1553-89del
XM_024453992.1:c.1553-89del XP_024309760.1:n.1553-89del
XM_024453993.1:c.1508-89del XP_024309761.1:n.1508-89del
XM_024453994.1:c.1508-89del XP_024309762.1:n.1508-89del
NM_015030.2:c.1508-89del MANE Select NP_055845.1:n.1508-89del