Canonical Allele Identifier: CA11693858

Gene: FAM13A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88855930A>G , CM000666.2:g.88855930A>G	GRCh38
NC_000004.11:g.89777081A>G , CM000666.1:g.89777081A>G	GRCh37
NC_000004.10:g.89996104A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264344.10:c.844-4747T>C MANE Select	ENSP00000264344.5:n.844-4747T>C
ENST00000264344.9:c.844-4747T>C	ENSP00000264344.5:n.844-4747T>C
ENST00000502459.5:n.1302-4747T>C
ENST00000511145.1:n.323T>C
ENST00000511976.5:c.216+50449T>C	ENSP00000421914.1:n.216+50449T>C
ENST00000512339.5:c.*309T>C	ENSP00000423800.1:n.*309T>C
NM_014883.3:c.844-4747T>C	NP_055698.2:n.844-4747T>C
XM_005262681.2:c.844-4747T>C	XP_005262738.1:n.844-4747T>C
XM_005262682.2:c.784-4747T>C	XP_005262739.1:n.784-4747T>C
XM_005262683.2:c.844-4747T>C	XP_005262740.1:n.844-4747T>C
XM_005262684.2:c.217-4747T>C	XP_005262741.1:n.217-4747T>C
XM_006714057.2:c.277-4747T>C	XP_006714120.1:n.277-4747T>C
XM_011531516.1:c.844-4747T>C	XP_011529818.1:n.844-4747T>C
XM_011531517.1:c.760-4747T>C	XP_011529819.1:n.760-4747T>C
XM_011531518.1:c.286-4747T>C	XP_011529820.1:n.286-4747T>C
XM_011531519.1:c.286-4747T>C	XP_011529821.1:n.286-4747T>C
XM_011531520.1:c.217-4747T>C	XP_011529822.1:n.217-4747T>C
XM_005262681.3:c.844-4747T>C	XP_005262738.1:n.844-4747T>C
XM_005262683.3:c.844-4747T>C	XP_005262740.1:n.844-4747T>C
XM_005262684.4:c.217-4747T>C	XP_005262741.1:n.217-4747T>C
XM_006714057.3:c.277-4747T>C	XP_006714120.1:n.277-4747T>C
XM_011531517.2:c.760-4747T>C	XP_011529819.1:n.760-4747T>C
XM_011531519.3:c.286-4747T>C	XP_011529821.1:n.286-4747T>C
XM_017007624.2:c.844-4747T>C	XP_016863113.1:n.844-4747T>C
XM_017007625.1:c.679-4747T>C	XP_016863114.1:n.679-4747T>C
XM_017007626.1:c.313-4747T>C	XP_016863115.1:n.313-4747T>C
XM_017007627.1:c.217-4747T>C	XP_016863116.1:n.217-4747T>C
XM_017007628.2:c.217-4747T>C	XP_016863117.1:n.217-4747T>C
XM_017007629.2:c.28-4747T>C	XP_016863118.1:n.28-4747T>C
XM_017007630.2:c.28-4747T>C	XP_016863119.1:n.28-4747T>C
XM_017007631.2:c.28-4747T>C	XP_016863120.1:n.28-4747T>C
XM_017007632.2:c.28-4747T>C	XP_016863121.1:n.28-4747T>C
XM_017007633.2:c.-120-4747T>C	XP_016863122.1:n.-120-4747T>C
XM_024453870.1:c.844-4747T>C	XP_024309638.1:n.844-4747T>C
NM_014883.4:c.844-4747T>C MANE Select	NP_055698.2:n.844-4747T>C