Canonical Allele Identifier: CA984207638
Gene: MYL4 HGNC NCBI

Linked Data

dbSNP Id: rs2064861958

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47222269_47222270insAAACCAGGCTTGGTTTGAAGGT , CM000679.2:g.47222269_47222270insAAACCAGGCTTGGTTTGAAGGT GRCh38
NC_000017.10:g.45299635_45299636insAAACCAGGCTTGGTTTGAAGGT , CM000679.1:g.45299635_45299636insAAACCAGGCTTGGTTTGAAGGT GRCh37
NC_000017.9:g.42654634_42654635insAAACCAGGCTTGGTTTGAAGGT NCBI36
NG_052847.1:g.18253_18254insAAACCAGGCTTGGTTTGAAGGT

Transcript Alleles

HGVS Amino-acid change
ENST00000354968.5:c.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT ENSP00000347055.1:n.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT
ENST00000393450.5:c.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT MANE Select ENSP00000377096.1:n.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT
ENST00000536623.6:c.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT ENSP00000442375.2:n.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT
ENST00000570671.1:c.199-111_199-110insAAACCAGGCTTGGTTTGAAGGT
ENST00000571981.5:c.*274-111_*274-110insAAACCAGGCTTGGTTTGAAGGT ENSP00000459035.1:n.*274-111_*274-110insAAACCAGGCTTGGTTTGAAGG...
ENST00000572316.5:c.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT ENSP00000461570.1:n.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT
ENST00000573747.6:c.*90-111_*90-110insAAACCAGGCTTGGTTTGAAGGT ENSP00000460734.1:n.*90-111_*90-110insAAACCAGGCTTGGTTTGAAGGT
ENST00000576874.5:c.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT ENSP00000458907.1:n.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT
NM_001002841.1:c.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT NP_001002841.1:n.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT
NM_002476.2:c.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT MANE Select NP_002467.1:n.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT
XM_005257391.3:c.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT XP_005257448.1:n.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT
XM_011524838.1:c.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT XP_011523140.1:n.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT
XM_011524839.1:c.278-111_278-110insAAACCAGGCTTGGTTTGAAGGT XP_011523141.1:n.278-111_278-110insAAACCAGGCTTGGTTTGAAGGT
XM_005257391.5:c.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT XP_005257448.1:n.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT
XM_011524839.2:c.581-111_581-110insAAACCAGGCTTGGTTTGAAGGT XP_011523141.2:n.581-111_581-110insAAACCAGGCTTGGTTTGAAGGT
XM_017024683.1:c.581-111_581-110insAAACCAGGCTTGGTTTGAAGGT XP_016880172.1:n.581-111_581-110insAAACCAGGCTTGGTTTGAAGGT
XM_024450766.1:c.581-111_581-110insAAACCAGGCTTGGTTTGAAGGT XP_024306534.1:n.581-111_581-110insAAACCAGGCTTGGTTTGAAGGT
NM_001002841.2:c.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT NP_001002841.1:n.488-111_488-110insAAACCAGGCTTGGTTTGAAGGT