Canonical Allele Identifier: CA355735939

Gene: MASP1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.187236513C>A , CM000665.2:g.187236513C>A	GRCh38
NC_000003.11:g.186954301C>A , CM000665.1:g.186954301C>A	GRCh37
NC_000003.10:g.188436995C>A	NCBI36
NG_029440.1:g.60510G>T , LRG_349:g.60510G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_139125.4:c.1358G>T MANE Select	NP_624302.1:p.Gly453Val
ENST00000296280.11:c.1358G>T MANE Select	ENSP00000296280.7:p.Gly453Val
NM_001879.6:c.1303+4968G>T MANE Plus Clinical	NP_001870.3:n.1303+4968G>T
ENST00000337774.10:c.1303+4968G>T MANE Plus Clinical	ENSP00000336792.5:n.1303+4968G>T
NM_001879.5:c.1303+4968G>T , LRG_349t2:c.1303+4968G>T	NP_001870.3:n.1303+4968G>T
NM_139125.3:c.1358G>T , LRG_349t3:c.1358G>T	NP_624302.1:p.Gly453Val
NR_033519.1:n.1516G>T
NR_033519.2:n.1231G>T
ENST00000296280.10:c.1358G>T	ENSP00000296280.6:p.Gly453Val
ENST00000337774.9:c.1303+4968G>T	ENSP00000336792.5:n.1303+4968G>T
ENST00000392472.6:c.1019G>T	ENSP00000376264.2:p.Gly340Val
ENST00000468121.1:n.177+4968G>T
ENST00000480349.1:n.3551G>T
ENST00000495249.1:n.67-126G>T
XM_006713700.2:c.1280G>T	XP_006713763.1:p.Gly427Val
XM_011512989.1:c.1379G>T	XP_011511291.1:p.Gly460Val
XM_011512989.2:c.1379G>T	XP_011511291.1:p.Gly460Val
XM_011512990.1:c.1324+4968G>T	XP_011511292.1:n.1324+4968G>T
XM_011512990.2:c.1324+4968G>T	XP_011511292.1:n.1324+4968G>T
XM_017006869.1:c.1280G>T	XP_016862358.1:p.Gly427Val
XM_017006870.2:c.1210+4968G>T	XP_016862359.1:n.1210+4968G>T
XM_017006871.1:c.1324+4968G>T	XP_016862360.1:n.1324+4968G>T
XM_017006872.1:c.1019G>T	XP_016862361.1:p.Gly340Val