Canonical Allele Identifier: CA1119758978

Gene: FAM135B

Linked Data

• gnomAD v3: 8-138492015-C-CCG
• gnomAD v4: 8-138492015-C-CCG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.138492015_138492016insCG , CM000670.2:g.138492015_138492016insCG	GRCh38
NC_000008.10:g.139504258_139504259insCG , CM000670.1:g.139504258_139504259insCG	GRCh37
NC_000008.9:g.139573440_139573441insCG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395297.6:c.-20+4655_-20+4656insCG MANE Select	ENSP00000378710.1:n.-20+4655_-20+4656insCG
ENST00000276737.10:c.-20+4655_-20+4656insCG	ENSP00000276737.6:n.-20+4655_-20+4656insCG
ENST00000395297.5:c.-20+4655_-20+4656insCG	ENSP00000378710.1:n.-20+4655_-20+4656insCG
NM_015912.3:c.-20+4655_-20+4656insCG	NP_056996.2:n.-20+4655_-20+4656insCG
XM_011517061.1:c.-165+4655_-165+4656insCG	XP_011515363.1:n.-165+4655_-165+4656insCG
XM_011517062.1:c.-20+4655_-20+4656insCG	XP_011515364.1:n.-20+4655_-20+4656insCG
NM_001362965.1:c.-20+5611_-20+5612insCG	NP_001349894.1:n.-20+5611_-20+5612insCG
XM_011517061.2:c.-165+4655_-165+4656insCG	XP_011515363.1:n.-165+4655_-165+4656insCG
NM_015912.4:c.-20+4655_-20+4656insCG MANE Select	NP_056996.2:n.-20+4655_-20+4656insCG
NM_001362965.2:c.-20+5611_-20+5612insCG	NP_001349894.1:n.-20+5611_-20+5612insCG