Canonical Allele Identifier: CA143814
Gene: MACROD2 HGNC NCBI
FLRT3 HGNC NCBI

Linked Data

ClinVar Variation Id: 50862
ClinVar RCV Id: RCV000043602
dbSNP Id: rs398124651

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.14327217T>C , CM000682.2:g.14327217T>C GRCh38
NC_000020.10:g.14307863T>C , CM000682.1:g.14307863T>C GRCh37
NC_000020.9:g.14255863T>C NCBI36
NG_033913.1:g.15451A>G
NG_054905.1:g.336718T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000684519.1:c.272-166262T>C (MACROD2) MANE Select ENSP00000507484.1:n.272-166262T>C
ENST00000341420.5:c.290A>G (FLRT3) MANE Select ENSP00000339912.4:p.Glu97Gly
ENST00000642719.1:c.272-166262T>C (MACROD2) ENSP00000496601.1:n.272-166262T>C
ENST00000217246.8:c.272-166262T>C (MACROD2) ENSP00000217246.4:n.272-166262T>C
ENST00000341420.4:c.290A>G (FLRT3) ENSP00000339912.4:p.Glu97Gly
ENST00000378053.3:c.290A>G (FLRT3) ENSP00000367292.3:p.Glu97Gly
ENST00000477147.5:n.541-166262T>C (MACROD2)
ENST00000490428.5:n.263-166262T>C (MACROD2)
ENST00000494602.5:n.299-166262T>C (MACROD2)
NM_013281.3:c.290A>G (FLRT3) NP_037413.1:p.Glu97Gly
NM_080676.5:c.272-166262T>C (MACROD2) NP_542407.2:n.272-166262T>C
NM_198391.2:c.290A>G (FLRT3) NP_938205.1:p.Glu97Gly
XM_005260682.3:c.290A>G (FLRT3) XP_005260739.1:p.Glu97Gly
XM_011529204.1:c.290A>G (FLRT3) XP_011527506.1:p.Glu97Gly
XM_011529205.1:c.290A>G (FLRT3) XP_011527507.1:p.Glu97Gly
NM_001351661.1:c.272-166262T>C (MACROD2) NP_001338590.1:n.272-166262T>C
NM_001351663.1:c.272-166262T>C (MACROD2) NP_001338592.1:n.272-166262T>C
XM_005260682.4:c.290A>G (FLRT3) XP_005260739.1:p.Glu97Gly
XM_011529204.2:c.290A>G (FLRT3) XP_011527506.1:p.Glu97Gly
XM_011529205.2:c.290A>G (FLRT3) XP_011527507.1:p.Glu97Gly
NM_198391.3:c.290A>G (FLRT3) MANE Select NP_938205.1:p.Glu97Gly
NM_001351661.2:c.272-166262T>C (MACROD2) MANE Select NP_001338590.1:n.272-166262T>C
NM_001351663.2:c.272-166262T>C (MACROD2) NP_001338592.1:n.272-166262T>C
NM_080676.6:c.272-166262T>C (MACROD2) NP_542407.2:n.272-166262T>C
NM_013281.4:c.290A>G (FLRT3) NP_037413.1:p.Glu97Gly