Canonical Allele Identifier: CA408296738

Gene: MACROD2 FLRT3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.14326508C>G , CM000682.2:g.14326508C>G	GRCh38
NC_000020.10:g.14307154C>G , CM000682.1:g.14307154C>G	GRCh37
NC_000020.9:g.14255154C>G	NCBI36
NG_033913.1:g.16160G>C
NG_054905.1:g.336009C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001351661.2:c.272-166971C>G (MACROD2) MANE Select	NP_001338590.1:n.272-166971C>G
NM_198391.3:c.999G>C (FLRT3) MANE Select	NP_938205.1:p.Met333Ile
ENST00000341420.5:c.999G>C (FLRT3) MANE Select	ENSP00000339912.4:p.Met333Ile
ENST00000684519.1:c.272-166971C>G (MACROD2) MANE Select	ENSP00000507484.1:n.272-166971C>G
NM_001351661.1:c.272-166971C>G (MACROD2)	NP_001338590.1:n.272-166971C>G
NM_001351663.1:c.272-166971C>G (MACROD2)	NP_001338592.1:n.272-166971C>G
NM_001351663.2:c.272-166971C>G (MACROD2)	NP_001338592.1:n.272-166971C>G
NM_013281.3:c.999G>C (FLRT3)	NP_037413.1:p.Met333Ile
NM_013281.4:c.999G>C (FLRT3)	NP_037413.1:p.Met333Ile
NM_080676.5:c.272-166971C>G (MACROD2)	NP_542407.2:n.272-166971C>G
NM_080676.6:c.272-166971C>G (MACROD2)	NP_542407.2:n.272-166971C>G
NM_198391.2:c.999G>C (FLRT3)	NP_938205.1:p.Met333Ile
ENST00000217246.8:c.272-166971C>G (MACROD2)	ENSP00000217246.4:n.272-166971C>G
ENST00000341420.4:c.999G>C (FLRT3)	ENSP00000339912.4:p.Met333Ile
ENST00000378053.3:c.999G>C (FLRT3)	ENSP00000367292.3:p.Met333Ile
ENST00000477147.5:n.541-166971C>G (MACROD2)
ENST00000490428.5:n.263-166971C>G (MACROD2)
ENST00000494602.5:n.299-166971C>G (MACROD2)
ENST00000642719.1:c.272-166971C>G (MACROD2)	ENSP00000496601.1:n.272-166971C>G
XM_005260682.3:c.999G>C (FLRT3)	XP_005260739.1:p.Met333Ile
XM_005260682.4:c.999G>C (FLRT3)	XP_005260739.1:p.Met333Ile
XM_011529204.1:c.999G>C (FLRT3)	XP_011527506.1:p.Met333Ile
XM_011529204.2:c.999G>C (FLRT3)	XP_011527506.1:p.Met333Ile
XM_011529205.1:c.999G>C (FLRT3)	XP_011527507.1:p.Met333Ile
XM_011529205.2:c.999G>C (FLRT3)	XP_011527507.1:p.Met333Ile