Canonical Allele Identifier: CA2390270907

Gene: FAM3B

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41326678_41326679delinsTG , CM000683.2:g.41326678_41326679delinsTG	GRCh38
NC_000021.8:g.42698605_42698606delinsTG , CM000683.1:g.42698605_42698606delinsTG	GRCh37
NC_000021.7:g.41620475_41620476delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357985.7:c.163+3612_163+3613delinsTG MANE Select	ENSP00000350673.2:n.163+3612_163+3613delinsTG
ENST00000357985.6:c.163+3612_163+3613delinsTG	ENSP00000350673.2:n.163+3612_163+3613delinsTG
ENST00000398646.3:c.232+3612_232+3613delinsTG	ENSP00000381641.3:n.232+3612_232+3613delinsTG
ENST00000398647.7:c.19+9780_19+9781delinsTG	ENSP00000381642.3:n.19+9780_19+9781delinsTG
ENST00000398652.7:c.280+3612_280+3613delinsTG	ENSP00000381646.3:n.280+3612_280+3613delinsTG
ENST00000479810.6:n.1764+3612_1764+3613delinsTG
ENST00000518236.1:n.205+3612_205+3613delinsTG
NM_058186.3:c.163+3612_163+3613delinsTG	NP_478066.3:n.163+3612_163+3613delinsTG
NM_206964.1:c.19+9780_19+9781delinsTG	NP_996847.1:n.19+9780_19+9781delinsTG
XM_011529648.1:c.163+3612_163+3613delinsTG	XP_011527950.1:n.163+3612_163+3613delinsTG
XM_011529649.1:c.205+3612_205+3613delinsTG	XP_011527951.1:n.205+3612_205+3613delinsTG
XR_937526.1:n.662+3612_662+3613delinsTG
XM_011529648.2:c.391+3612_391+3613delinsTG	XP_011527950.2:n.391+3612_391+3613delinsTG
XM_011529649.2:c.205+3612_205+3613delinsTG	XP_011527951.1:n.205+3612_205+3613delinsTG
XR_937526.2:n.663+3612_663+3613delinsTG
NM_058186.4:c.163+3612_163+3613delinsTG MANE Select	NP_478066.3:n.163+3612_163+3613delinsTG
NM_206964.2:c.19+9780_19+9781delinsTG	NP_996847.1:n.19+9780_19+9781delinsTG