Canonical Allele Identifier: CA656612195

Gene: MYO15A

Linked Data

• COSMIC: COSN26557713

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18150349G>T , CM000679.2:g.18150349G>T	GRCh38
NC_000017.10:g.18053663G>T , CM000679.1:g.18053663G>T	GRCh37
NC_000017.9:g.17994388G>T	NCBI36
NG_011634.1:g.46644G>T
NG_011634.2:g.46644G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647165.2:c.7213-80G>T MANE Select	ENSP00000495481.1:n.7213-80G>T
ENST00000205890.9:c.7213-80G>T	ENSP00000205890.5:n.7213-80G>T
ENST00000615845.4:c.7213-80G>T	ENSP00000481642.1:n.7213-80G>T
NM_016239.3:c.7213-80G>T	NP_057323.3:n.7213-80G>T
XM_011523917.1:c.6888-80G>T	XP_011522219.1:n.6888-80G>T
XM_011523921.1:c.7207-80G>T	XP_011522223.1:n.7207-80G>T
XR_934037.1:n.7547-80G>T
XR_934038.1:n.7499-80G>T
XR_934293.1:n.434+1254C>A
XR_934294.1:n.435-576C>A
XR_934295.1:n.253+1254C>A
XM_017024714.2:c.7153-80G>T	XP_016880203.1:n.7153-80G>T
XM_017024715.2:c.7216-80G>T	XP_016880204.1:n.7216-80G>T
XR_934293.2:n.377+1254C>A
XR_934294.2:n.378-576C>A
NM_016239.4:c.7213-80G>T MANE Select	NP_057323.3:n.7213-80G>T