Canonical Allele Identifier: CA1823684528

Gene: FAM135B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.138491983A= , CM000670.2:g.138491983A=	GRCh38
NC_000008.10:g.139504226A= , CM000670.1:g.139504226A=	GRCh37
NC_000008.9:g.139573408A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395297.6:c.-20+4688T= MANE Select	ENSP00000378710.1:n.-20+4688T=
ENST00000276737.10:c.-20+4688T=	ENSP00000276737.6:n.-20+4688T=
ENST00000395297.5:c.-20+4688T=	ENSP00000378710.1:n.-20+4688T=
NM_015912.3:c.-20+4688T=	NP_056996.2:n.-20+4688T=
XM_011517061.1:c.-165+4688T=	XP_011515363.1:n.-165+4688T=
XM_011517062.1:c.-20+4688T=	XP_011515364.1:n.-20+4688T=
NM_001362965.1:c.-20+5644T=	NP_001349894.1:n.-20+5644T=
XM_011517061.2:c.-165+4688T=	XP_011515363.1:n.-165+4688T=
NM_015912.4:c.-20+4688T= MANE Select	NP_056996.2:n.-20+4688T=
NM_001362965.2:c.-20+5644T=	NP_001349894.1:n.-20+5644T=