Canonical Allele Identifier: CA1798105

Gene: LYG2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.99246784A>C , CM000664.2:g.99246784A>C	GRCh38
NC_000002.11:g.99863247A>C , CM000664.1:g.99863247A>C	GRCh37
NC_000002.10:g.99229679A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_175735.4:c.80T>G MANE Select	NP_783862.2:p.Met27Arg
ENST00000333017.7:c.80T>G MANE Select	ENSP00000327533.2:p.Met27Arg
NM_175735.3:c.80T>G	NP_783862.2:p.Met27Arg
ENST00000333017.6:c.80T>G	ENSP00000327533.2:p.Met27Arg
ENST00000409238.5:c.80T>G	ENSP00000386939.1:p.Met27Arg
ENST00000409679.5:c.80T>G	ENSP00000386381.1:p.Met27Arg
ENST00000423306.1:c.80T>G	ENSP00000405439.1:p.Met27Arg
ENST00000423800.5:c.80T>G	ENSP00000390357.1:p.Met27Arg
ENST00000424491.5:c.*292+30670A>C	ENSP00000390891.1:n.*292+30670A>C
ENST00000626374.2:c.80T>G	ENSP00000487012.1:p.Met27Arg
XM_011510900.1:c.257T>G	XP_011509202.1:p.Met86Arg
XM_011510901.1:c.80T>G	XP_011509203.1:p.Met27Arg
XM_011510902.1:c.80T>G	XP_011509204.1:p.Met27Arg
XM_017003751.2:c.80T>G	XP_016859240.1:p.Met27Arg
XM_024452782.1:c.80T>G	XP_024308550.1:p.Met27Arg