Canonical Allele Identifier: CA2544700166

Gene: F2R

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.76727575_76727576insCG , CM000667.2:g.76727575_76727576insCG	GRCh38
NC_000005.9:g.76023400_76023401insCG , CM000667.1:g.76023400_76023401insCG	GRCh37
NC_000005.8:g.76059156_76059157insCG	NCBI36
NG_032906.1:g.16533_16534insCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000319211.5:c.89-4739_89-4738insCG MANE Select	ENSP00000321326.4:n.89-4739_89-4738insCG
ENST00000319211.4:c.89-4739_89-4738insCG	ENSP00000321326.4:n.89-4739_89-4738insCG
NM_001311313.1:c.-397-1137_-397-1136insCG	NP_001298242.1:n.-397-1137_-397-1136insCG...
NM_001992.3:c.89-4739_89-4738insCG	NP_001983.2:n.89-4739_89-4738insCG
NM_001992.4:c.89-4739_89-4738insCG	NP_001983.2:n.89-4739_89-4738insCG
NM_001992.5:c.89-4739_89-4738insCG MANE Select	NP_001983.2:n.89-4739_89-4738insCG
NM_001311313.2:c.-397-1137_-397-1136insCG	NP_001298242.1:n.-397-1137_-397-1136insCG...