Canonical Allele Identifier: CA500433871

Gene: MYL4

Linked Data

• MyVariant Identifiers: chr17:g.45299100C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47221734C>T , CM000679.2:g.47221734C>T	GRCh38
NC_000017.10:g.45299100C>T , CM000679.1:g.45299100C>T	GRCh37
NC_000017.9:g.42654099C>T	NCBI36
NG_052847.1:g.17718C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354968.5:c.366C>T	ENSP00000347055.1:p.His122=
ENST00000393450.5:c.366C>T MANE Select	ENSP00000377096.1:p.His122=
ENST00000536623.6:c.366C>T	ENSP00000442375.2:p.His122=
ENST00000570671.1:c.77C>T
ENST00000570772.5:c.*152C>T	ENSP00000458194.1:n.*152C>T
ENST00000571981.5:c.*152C>T	ENSP00000459035.1:n.*152C>T
ENST00000572303.1:c.459C>T	ENSP00000461747.1:p.His153=
ENST00000572316.5:c.366C>T	ENSP00000461570.1:p.His122=
ENST00000573747.6:c.316C>T	ENSP00000460734.1:p.His106Tyr
ENST00000576874.5:c.366C>T	ENSP00000458907.1:p.His122=
NM_001002841.1:c.366C>T	NP_001002841.1:p.His122=
NM_002476.2:c.366C>T MANE Select	NP_002467.1:p.His122=
XM_005257391.3:c.366C>T	XP_005257448.1:p.His122=
XM_011524838.1:c.366C>T	XP_011523140.1:p.His122=
XM_011524839.1:c.156C>T	XP_011523141.1:p.His52=
XM_005257391.5:c.366C>T	XP_005257448.1:p.His122=
XM_011524839.2:c.459C>T	XP_011523141.2:p.His153=
XM_017024683.1:c.459C>T	XP_016880172.1:p.His153=
XM_024450766.1:c.459C>T	XP_024306534.1:p.His153=
NM_001002841.2:c.366C>T	NP_001002841.1:p.His122=