Canonical Allele Identifier: CA8622715
Gene: MYL4 HGNC NCBI

Linked Data

ClinVar Variation Id: 476202
dbSNP Id: rs114024716

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47221678G>A , CM000679.2:g.47221678G>A GRCh38
NC_000017.10:g.45299044G>A , CM000679.1:g.45299044G>A GRCh37
NC_000017.9:g.42654043G>A NCBI36
NG_052847.1:g.17662G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000354968.5:c.314-4G>A ENSP00000347055.1:n.314-4G>A
ENST00000393450.5:c.314-4G>A MANE Select ENSP00000377096.1:n.314-4G>A
ENST00000536623.6:c.314-4G>A ENSP00000442375.2:n.314-4G>A
ENST00000570671.1:c.25-4G>A
ENST00000570772.5:c.*100-4G>A ENSP00000458194.1:n.*100-4G>A
ENST00000571981.5:c.*100-4G>A ENSP00000459035.1:n.*100-4G>A
ENST00000572303.1:c.407-4G>A ENSP00000461747.1:n.407-4G>A
ENST00000572316.5:c.314-4G>A ENSP00000461570.1:n.314-4G>A
ENST00000573747.6:c.314-54G>A ENSP00000460734.1:n.314-54G>A
ENST00000576874.5:c.314-4G>A ENSP00000458907.1:n.314-4G>A
NM_001002841.1:c.314-4G>A NP_001002841.1:n.314-4G>A
NM_002476.2:c.314-4G>A MANE Select NP_002467.1:n.314-4G>A
XM_005257391.3:c.314-4G>A XP_005257448.1:n.314-4G>A
XM_011524838.1:c.314-4G>A XP_011523140.1:n.314-4G>A
XM_011524839.1:c.104-4G>A XP_011523141.1:n.104-4G>A
XM_005257391.5:c.314-4G>A XP_005257448.1:n.314-4G>A
XM_011524839.2:c.407-4G>A XP_011523141.2:n.407-4G>A
XM_017024683.1:c.407-4G>A XP_016880172.1:n.407-4G>A
XM_024450766.1:c.407-4G>A XP_024306534.1:n.407-4G>A
NM_001002841.2:c.314-4G>A NP_001002841.1:n.314-4G>A