Canonical Allele Identifier: CA500433924

Gene: MYL4

Linked Data

• MyVariant Identifiers: chr17:g.45299142G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47221776G>T , CM000679.2:g.47221776G>T	GRCh38
NC_000017.10:g.45299142G>T , CM000679.1:g.45299142G>T	GRCh37
NC_000017.9:g.42654141G>T	NCBI36
NG_052847.1:g.17760G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000354968.5:c.408G>T	ENSP00000347055.1:p.Val136=
ENST00000393450.5:c.408G>T MANE Select	ENSP00000377096.1:p.Val136=
ENST00000536623.6:c.408G>T	ENSP00000442375.2:p.Val136=
ENST00000570671.1:c.119G>T
ENST00000570772.5:c.*194G>T	ENSP00000458194.1:n.*194G>T
ENST00000571981.5:c.*194G>T	ENSP00000459035.1:n.*194G>T
ENST00000572303.1:c.501G>T	ENSP00000461747.1:p.Val167=
ENST00000572316.5:c.408G>T	ENSP00000461570.1:p.Val136=
ENST00000573747.6:c.*10G>T	ENSP00000460734.1:n.*10G>T
ENST00000576874.5:c.408G>T	ENSP00000458907.1:p.Val136=
NM_001002841.1:c.408G>T	NP_001002841.1:p.Val136=
NM_002476.2:c.408G>T MANE Select	NP_002467.1:p.Val136=
XM_005257391.3:c.408G>T	XP_005257448.1:p.Val136=
XM_011524838.1:c.408G>T	XP_011523140.1:p.Val136=
XM_011524839.1:c.198G>T	XP_011523141.1:p.Val66=
XM_005257391.5:c.408G>T	XP_005257448.1:p.Val136=
XM_011524839.2:c.501G>T	XP_011523141.2:p.Val167=
XM_017024683.1:c.501G>T	XP_016880172.1:p.Val167=
XM_024450766.1:c.501G>T	XP_024306534.1:p.Val167=
NM_001002841.2:c.408G>T	NP_001002841.1:p.Val136=