Canonical Allele Identifier: CA251515

Gene: FECH

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57573246_57573365del , CM000680.2:g.57573246_57573365del	GRCh38
NC_000018.9:g.55240478_55240597del , CM000680.1:g.55240478_55240597del	GRCh37
NC_000018.8:g.53391476_53391595del	NCBI36
NG_008175.1:g.18374_18493del

Transcript Alleles

HGVS	Amino-acid change
ENST00000592699.6:c.196_314+1del
ENST00000682485.1:n.308_426+1del
ENST00000262093.11:c.196_314+1del
ENST00000382873.8:c.-21_98+1del
ENST00000651787.1:n.302_420+1del
ENST00000652755.1:c.214_332+1del
ENST00000262093.9:c.196_314+1del
ENST00000382873.7:c.214_332+1del
ENST00000585494.5:c.196_314+1del
ENST00000585699.1:n.148_266+1del
ENST00000585747.1:c.196_314+1del
ENST00000585878.1:n.248_367del
ENST00000591215.5:c.-21_98+1del
ENST00000592111.1:n.197_316del
ENST00000592699.5:c.196_314+1del
NM_000140.3:c.196_314+1del
NM_001012515.2:c.214_332+1del
XM_011525881.1:c.214_332+1del
XM_011525882.1:c.-21_98+1del
NM_000140.4:c.196_314+1del
NM_001012515.3:c.214_332+1del
XM_011525882.2:c.-21_98+1del
XM_017025614.2:c.196_314+1del
NM_000140.5:c.196_314+1del
NM_001012515.4:c.214_332+1del
NM_001371094.1:c.196_314+1del
NM_001371095.1:c.-21_98+1del
NM_001374778.1:c.196_314+1del