Canonical Allele Identifier: CA1474877690

Gene: FAM13A FAM13A-AS1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.88726273T>G , CM000666.2:g.88726273T>G	GRCh38
NC_000004.11:g.89647424T>G , CM000666.1:g.89647424T>G	GRCh37
NC_000004.10:g.89866447T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264344.10:c.*2260A>C (FAM13A) MANE Select	ENSP00000264344.5:n.*2260A>C
ENST00000264344.9:c.*2260A>C (FAM13A)	ENSP00000264344.5:n.*2260A>C
ENST00000395002.6:c.*2260A>C (FAM13A)	ENSP00000378450.2:n.*2260A>C
NM_001015045.2:c.*2260A>C (FAM13A)	NP_001015045.1:n.*2260A>C
NM_001265578.1:c.*2260A>C (FAM13A)	NP_001252507.1:n.*2260A>C
NM_001265579.1:c.*2260A>C (FAM13A)	NP_001252508.1:n.*2260A>C
NM_001265580.1:c.*2260A>C (FAM13A)	NP_001252509.1:n.*2260A>C
NM_014883.3:c.*2260A>C (FAM13A)	NP_055698.2:n.*2260A>C
NR_002806.2:n.942-1562T>G (FAM13A-AS1)
XM_005262681.2:c.*2260A>C (FAM13A)	XP_005262738.1:n.*2260A>C
XM_005262682.2:c.*2260A>C (FAM13A)	XP_005262739.1:n.*2260A>C
XM_005262683.2:c.*2260A>C (FAM13A)	XP_005262740.1:n.*2260A>C
XM_005262684.2:c.*2260A>C (FAM13A)	XP_005262741.1:n.*2260A>C
XM_006714057.2:c.*2260A>C (FAM13A)	XP_006714120.1:n.*2260A>C
XM_011531516.1:c.*2260A>C (FAM13A)	XP_011529818.1:n.*2260A>C
XM_011531517.1:c.*2260A>C (FAM13A)	XP_011529819.1:n.*2260A>C
XM_011531518.1:c.*2260A>C (FAM13A)	XP_011529820.1:n.*2260A>C
XM_011531519.1:c.*2260A>C (FAM13A)	XP_011529821.1:n.*2260A>C
XM_011531520.1:c.*2260A>C (FAM13A)	XP_011529822.1:n.*2260A>C
XM_005262681.3:c.*2260A>C (FAM13A)	XP_005262738.1:n.*2260A>C
XM_005262683.3:c.*2260A>C (FAM13A)	XP_005262740.1:n.*2260A>C
XM_005262684.4:c.*2260A>C (FAM13A)	XP_005262741.1:n.*2260A>C
XM_006714057.3:c.*2260A>C (FAM13A)	XP_006714120.1:n.*2260A>C
XM_011531517.2:c.*2260A>C (FAM13A)	XP_011529819.1:n.*2260A>C
XM_011531519.3:c.*2260A>C (FAM13A)	XP_011529821.1:n.*2260A>C
XM_017007624.2:c.*2260A>C (FAM13A)	XP_016863113.1:n.*2260A>C
XM_017007625.1:c.*2260A>C (FAM13A)	XP_016863114.1:n.*2260A>C
XM_017007626.1:c.*2260A>C (FAM13A)	XP_016863115.1:n.*2260A>C
XM_017007627.1:c.*2260A>C (FAM13A)	XP_016863116.1:n.*2260A>C
XM_017007628.2:c.*2260A>C (FAM13A)	XP_016863117.1:n.*2260A>C
XM_017007629.2:c.*2260A>C (FAM13A)	XP_016863118.1:n.*2260A>C
XM_017007630.2:c.*2260A>C (FAM13A)	XP_016863119.1:n.*2260A>C
XM_017007631.2:c.*2260A>C (FAM13A)	XP_016863120.1:n.*2260A>C
XM_017007632.2:c.*2260A>C (FAM13A)	XP_016863121.1:n.*2260A>C
XM_017007633.2:c.*2260A>C (FAM13A)	XP_016863122.1:n.*2260A>C
XM_017007634.2:c.*2260A>C (FAM13A)	XP_016863123.1:n.*2260A>C
NM_014883.4:c.*2260A>C (FAM13A) MANE Select	NP_055698.2:n.*2260A>C
NM_001015045.3:c.*2260A>C (FAM13A)	NP_001015045.1:n.*2260A>C
NM_001265578.2:c.*2260A>C (FAM13A)	NP_001252507.1:n.*2260A>C
NM_001265579.2:c.*2260A>C (FAM13A)	NP_001252508.1:n.*2260A>C
NM_001265580.2:c.*2260A>C (FAM13A)	NP_001252509.1:n.*2260A>C