Canonical Allele Identifier: CA1119758961

Gene: FAM135B

Linked Data

• gnomAD v3: 8-138492004-CATGGGAAAT-C
• gnomAD v4: 8-138492004-CATGGGAAAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.138492005_138492013del , CM000670.2:g.138492005_138492013del	GRCh38
NC_000008.10:g.139504248_139504256del , CM000670.1:g.139504248_139504256del	GRCh37
NC_000008.9:g.139573430_139573438del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395297.6:c.-20+4658_-20+4666del MANE Select	ENSP00000378710.1:n.-20+4658_-20+4666del
ENST00000276737.10:c.-20+4658_-20+4666del	ENSP00000276737.6:n.-20+4658_-20+4666del
ENST00000395297.5:c.-20+4658_-20+4666del	ENSP00000378710.1:n.-20+4658_-20+4666del
NM_015912.3:c.-20+4658_-20+4666del	NP_056996.2:n.-20+4658_-20+4666del
XM_011517061.1:c.-165+4658_-165+4666del	XP_011515363.1:n.-165+4658_-165+4666del
XM_011517062.1:c.-20+4658_-20+4666del	XP_011515364.1:n.-20+4658_-20+4666del
NM_001362965.1:c.-20+5614_-20+5622del	NP_001349894.1:n.-20+5614_-20+5622del
XM_011517061.2:c.-165+4658_-165+4666del	XP_011515363.1:n.-165+4658_-165+4666del
NM_015912.4:c.-20+4658_-20+4666del MANE Select	NP_056996.2:n.-20+4658_-20+4666del
NM_001362965.2:c.-20+5614_-20+5622del	NP_001349894.1:n.-20+5614_-20+5622del