Canonical Allele Identifier: CA1823684552

Gene: FAM135B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.138492000A= , CM000670.2:g.138492000A=	GRCh38
NC_000008.10:g.139504243A= , CM000670.1:g.139504243A=	GRCh37
NC_000008.9:g.139573425A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000395297.6:c.-20+4671T= MANE Select	ENSP00000378710.1:n.-20+4671T=
ENST00000276737.10:c.-20+4671T=	ENSP00000276737.6:n.-20+4671T=
ENST00000395297.5:c.-20+4671T=	ENSP00000378710.1:n.-20+4671T=
NM_015912.3:c.-20+4671T=	NP_056996.2:n.-20+4671T=
XM_011517061.1:c.-165+4671T=	XP_011515363.1:n.-165+4671T=
XM_011517062.1:c.-20+4671T=	XP_011515364.1:n.-20+4671T=
NM_001362965.1:c.-20+5627T=	NP_001349894.1:n.-20+5627T=
XM_011517061.2:c.-165+4671T=	XP_011515363.1:n.-165+4671T=
NM_015912.4:c.-20+4671T= MANE Select	NP_056996.2:n.-20+4671T=
NM_001362965.2:c.-20+5627T=	NP_001349894.1:n.-20+5627T=