Canonical Allele Identifier: CA10320128
Community Standard Title: NM_033200.3(LMF2):c.311A>G (p.Tyr104Cys)
Gene: LMF2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50506819T>C , CM000684.2:g.50506819T>C GRCh38
NC_000022.10:g.50945248T>C , CM000684.1:g.50945248T>C GRCh37
NC_000022.9:g.49292114T>C NCBI36
NG_021419.1:g.3604T>C

Transcript Alleles

HGVS Amino-acid Change
NM_033200.3:c.311A>G MANE Select NP_149977.2:p.Tyr104Cys
ENST00000474879.7:c.311A>G MANE Select ENSP00000424381.1:p.Tyr104Cys
NM_001363816.1:c.236A>G NP_001350745.1:p.Tyr79Cys
NM_001363816.2:c.236A>G NP_001350745.1:p.Tyr79Cys
NM_033200.2:c.311A>G NP_149977.2:p.Tyr104Cys
ENST00000216080.5:c.236A>G ENSP00000216080.5:p.Tyr79Cys
ENST00000474879.6:c.311A>G ENSP00000424381.1:p.Tyr104Cys
ENST00000505981.5:n.241A>G
ENST00000507607.1:n.432A>G
XM_005261955.2:c.236A>G XP_005262012.1:p.Tyr79Cys
XM_006724426.2:c.231A>G XP_006724489.1:p.Leu77=
XM_006724426.3:c.231A>G XP_006724489.1:p.Leu77=
XM_006724427.2:c.231A>G XP_006724490.1:p.Leu77=
XM_006724427.3:c.231A>G XP_006724490.1:p.Leu77=
XM_017029077.2:c.311A>G XP_016884566.1:p.Tyr104Cys
XR_001755368.2:n.417A>G
XR_938349.1:n.476A>G
XR_938349.3:n.417A>G