Canonical Allele Identifier: CA400022288
Gene: MYL4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47221745A>G , CM000679.2:g.47221745A>G GRCh38
NC_000017.10:g.45299111A>G , CM000679.1:g.45299111A>G GRCh37
NC_000017.9:g.42654110A>G NCBI36
NG_052847.1:g.17729A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000354968.5:c.377A>G ENSP00000347055.1:p.Asn126Ser
ENST00000393450.5:c.377A>G MANE Select ENSP00000377096.1:p.Asn126Ser
ENST00000536623.6:c.377A>G ENSP00000442375.2:p.Asn126Ser
ENST00000570671.1:c.88A>G
ENST00000570772.5:c.*163A>G ENSP00000458194.1:n.*163A>G
ENST00000571981.5:c.*163A>G ENSP00000459035.1:n.*163A>G
ENST00000572303.1:c.470A>G ENSP00000461747.1:p.Asn157Ser
ENST00000572316.5:c.377A>G ENSP00000461570.1:p.Asn126Ser
ENST00000573747.6:c.327A>G ENSP00000460734.1:p.Gln109=
ENST00000576874.5:c.377A>G ENSP00000458907.1:p.Asn126Ser
NM_001002841.1:c.377A>G NP_001002841.1:p.Asn126Ser
NM_002476.2:c.377A>G MANE Select NP_002467.1:p.Asn126Ser
XM_005257391.3:c.377A>G XP_005257448.1:p.Asn126Ser
XM_011524838.1:c.377A>G XP_011523140.1:p.Asn126Ser
XM_011524839.1:c.167A>G XP_011523141.1:p.Asn56Ser
XM_005257391.5:c.377A>G XP_005257448.1:p.Asn126Ser
XM_011524839.2:c.470A>G XP_011523141.2:p.Asn157Ser
XM_017024683.1:c.470A>G XP_016880172.1:p.Asn157Ser
XM_024450766.1:c.470A>G XP_024306534.1:p.Asn157Ser
NM_001002841.2:c.377A>G NP_001002841.1:p.Asn126Ser