Canonical Allele Identifier: CA1607542157
Gene: LYRM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.5260703A= , CM000668.2:g.5260703A= GRCh38
NC_000006.11:g.5260936A= , CM000668.1:g.5260936A= GRCh37
NC_000006.10:g.5205935A= NCBI36
NG_033003.1:g.4353A=
NG_051651.1:g.5248T=
NG_033003.2:g.4353A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330636.9:c.31T= MANE Select ENSP00000418787.1:p.Ser11=
ENST00000330636.8:c.31T= ENSP00000418787.1:p.Ser11=
ENST00000455814.2:n.19T=
ENST00000464010.5:c.31T= ENSP00000420026.1:p.Ser11=
ENST00000468929.5:c.31T= ENSP00000418321.1:p.Ser11=
ENST00000480566.5:c.31T= ENSP00000419928.1:p.Ser11=
ENST00000500576.4:c.31T= ENSP00000443900.3:p.Ser11=
NM_001164840.2:c.31T= NP_001158312.1:p.Ser11=
NM_001164841.2:c.31T= NP_001158313.1:p.Ser11=
NM_020408.5:c.31T= NP_065141.3:p.Ser11=
NR_104417.1:n.248T=
NR_104418.1:n.248T=
XM_005249237.3:c.31T= XP_005249294.1:p.Ser11=
XM_005249239.2:c.31T= XP_005249296.1:p.Ser11=
XM_006715151.1:c.31T= XP_006715214.1:p.Ser11=
XM_011514758.1:c.31T= XP_011513060.1:p.Ser11=
NM_001318782.1:c.31T= NP_001305711.1:p.Ser11=
NM_001318783.1:c.31T= NP_001305712.1:p.Ser11=
NR_134856.1:n.248T=
XM_017011083.2:c.31T= XP_016866572.1:p.Ser11=
XM_017011084.2:c.31T= XP_016866573.1:p.Ser11=
NM_001164840.3:c.31T= NP_001158312.1:p.Ser11=
NM_001164841.3:c.31T= NP_001158313.1:p.Ser11=
NM_020408.6:c.31T= MANE Select NP_065141.3:p.Ser11=
NR_104417.2:n.248T=