Canonical Allele Identifier: CA4889138

Gene: FAM135B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.138148544C>T , CM000670.2:g.138148544C>T	GRCh38
NC_000008.10:g.139160787C>T , CM000670.1:g.139160787C>T	GRCh37
NC_000008.9:g.139229969C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467365.2:n.1250G>A
ENST00000395297.6:c.3424G>A MANE Select	ENSP00000378710.1:p.Val1142Ile
ENST00000276737.10:c.3320G>A	ENSP00000276737.6:p.Gly1107Asp
ENST00000395295.2:n.292G>A
ENST00000395297.5:c.3424G>A	ENSP00000378710.1:p.Val1142Ile
ENST00000467365.1:c.1250G>A	ENSP00000430088.1:p.Gly417Asp
ENST00000482951.6:c.*3370G>A	ENSP00000429874.1:n.*3370G>A
NM_015912.3:c.3424G>A	NP_056996.2:p.Val1142Ile
XM_011517056.1:c.3436G>A	XP_011515358.1:p.Val1146Ile
XM_011517057.1:c.3436G>A	XP_011515359.1:p.Val1146Ile
XM_011517058.1:c.3436G>A	XP_011515360.1:p.Val1146Ile
XM_011517059.1:c.3436G>A	XP_011515361.1:p.Val1146Ile
XM_011517060.1:c.3436G>A	XP_011515362.1:p.Val1146Ile
XM_011517061.1:c.3436G>A	XP_011515363.1:p.Val1146Ile
XM_011517062.1:c.3436G>A	XP_011515364.1:p.Val1146Ile
XM_011517063.1:c.3436G>A	XP_011515365.1:p.Val1146Ile
XM_011517064.1:c.3424G>A	XP_011515366.1:p.Val1142Ile
XM_011517065.1:c.3388G>A	XP_011515367.1:p.Val1130Ile
XM_011517066.1:c.3436G>A	XP_011515368.1:p.Val1146Ile
XM_011517067.1:c.3436G>A	XP_011515369.1:p.Val1146Ile
XM_011517068.1:c.3127G>A	XP_011515370.1:p.Val1043Ile
XM_011517069.1:c.3070G>A	XP_011515371.1:p.Val1024Ile
XM_011517070.1:c.3436G>A	XP_011515372.1:p.Val1146Ile
XM_011517071.1:c.3424G>A	XP_011515373.1:p.Val1142Ile
XM_011517072.1:c.2833G>A	XP_011515374.1:p.Val945Ile
XM_011517073.1:c.2737G>A	XP_011515375.1:p.Val913Ile
XM_011517074.1:c.2689G>A	XP_011515376.1:p.Val897Ile
NM_001362965.1:c.3424G>A	NP_001349894.1:p.Val1142Ile
XM_011517056.2:c.3436G>A	XP_011515358.1:p.Val1146Ile
XM_011517058.2:c.3436G>A	XP_011515360.1:p.Val1146Ile
XM_011517060.2:c.3436G>A	XP_011515362.1:p.Val1146Ile
XM_011517061.2:c.3436G>A	XP_011515363.1:p.Val1146Ile
XM_011517063.2:c.3436G>A	XP_011515365.1:p.Val1146Ile
XM_011517064.2:c.3424G>A	XP_011515366.1:p.Val1142Ile
XM_011517068.2:c.3127G>A	XP_011515370.1:p.Val1043Ile
XM_011517069.2:c.3070G>A	XP_011515371.1:p.Val1024Ile
XM_011517070.2:c.3436G>A	XP_011515372.1:p.Val1146Ile
XM_011517072.2:c.2833G>A	XP_011515374.1:p.Val945Ile
XM_011517073.2:c.2737G>A	XP_011515375.1:p.Val913Ile
XM_017013471.1:c.3379G>A	XP_016868960.1:p.Val1127Ile
XR_001745531.1:n.4415G>A
XR_001745532.1:n.4404G>A
NM_015912.4:c.3424G>A MANE Select	NP_056996.2:p.Val1142Ile
NM_001362965.2:c.3424G>A	NP_001349894.1:p.Val1142Ile