Canonical Allele Identifier: CA498202760

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18053757A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18150443A>G , CM000679.2:g.18150443A>G	GRCh38
NC_000017.10:g.18053757A>G , CM000679.1:g.18053757A>G	GRCh37
NC_000017.9:g.17994482A>G	NCBI36
NG_011634.1:g.46738A>G
NG_011634.2:g.46738A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7227A>G MANE Select	ENSP00000495481.1:p.Pro2409=
ENST00000205890.9:c.7227A>G	ENSP00000205890.5:p.Pro2409=
ENST00000615845.4:c.7227A>G	ENSP00000481642.1:p.Pro2409=
NM_016239.3:c.7227A>G	NP_057323.3:p.Pro2409=
XM_011523917.1:c.6902A>G	XP_011522219.1:p.Gln2301Arg
XM_011523921.1:c.7221A>G	XP_011522223.1:p.Pro2407=
XR_934037.1:n.7561A>G
XR_934038.1:n.7513A>G
XR_934293.1:n.434+1160T>C
XR_934294.1:n.435-670T>C
XR_934295.1:n.253+1160T>C
XM_017024714.2:c.7167A>G	XP_016880203.1:p.Pro2389=
XM_017024715.2:c.7230A>G	XP_016880204.1:p.Pro2410=
XR_934293.2:n.377+1160T>C
XR_934294.2:n.378-670T>C
NM_016239.4:c.7227A>G MANE Select	NP_057323.3:p.Pro2409=