Canonical Allele Identifier: CA1823684452

Gene: FAM135B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.138491912G= , CM000670.2:g.138491912G=	GRCh38
NC_000008.10:g.139504155G= , CM000670.1:g.139504155G=	GRCh37
NC_000008.9:g.139573337G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000395297.6:c.-20+4759C= MANE Select	ENSP00000378710.1:n.-20+4759C=
ENST00000276737.10:c.-20+4759C=	ENSP00000276737.6:n.-20+4759C=
ENST00000395297.5:c.-20+4759C=	ENSP00000378710.1:n.-20+4759C=
NM_015912.3:c.-20+4759C=	NP_056996.2:n.-20+4759C=
XM_011517061.1:c.-165+4759C=	XP_011515363.1:n.-165+4759C=
XM_011517062.1:c.-20+4759C=	XP_011515364.1:n.-20+4759C=
NM_001362965.1:c.-20+5715C=	NP_001349894.1:n.-20+5715C=
XM_011517061.2:c.-165+4759C=	XP_011515363.1:n.-165+4759C=
NM_015912.4:c.-20+4759C= MANE Select	NP_056996.2:n.-20+4759C=
NM_001362965.2:c.-20+5715C=	NP_001349894.1:n.-20+5715C=