Canonical Allele Identifier: CA2636439867

Gene: MYO15A

Linked Data

• gnomAD v4: 17-18150370-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18150370C>T , CM000679.2:g.18150370C>T	GRCh38
NC_000017.10:g.18053684C>T , CM000679.1:g.18053684C>T	GRCh37
NC_000017.9:g.17994409C>T	NCBI36
NG_011634.1:g.46665C>T
NG_011634.2:g.46665C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000647165.2:c.7213-59C>T MANE Select	ENSP00000495481.1:n.7213-59C>T
ENST00000205890.9:c.7213-59C>T	ENSP00000205890.5:n.7213-59C>T
ENST00000615845.4:c.7213-59C>T	ENSP00000481642.1:n.7213-59C>T
NM_016239.3:c.7213-59C>T	NP_057323.3:n.7213-59C>T
XM_011523917.1:c.6888-59C>T	XP_011522219.1:n.6888-59C>T
XM_011523921.1:c.7207-59C>T	XP_011522223.1:n.7207-59C>T
XR_934037.1:n.7547-59C>T
XR_934038.1:n.7499-59C>T
XR_934293.1:n.434+1233G>A
XR_934294.1:n.435-597G>A
XR_934295.1:n.253+1233G>A
XM_017024714.2:c.7153-59C>T	XP_016880203.1:n.7153-59C>T
XM_017024715.2:c.7216-59C>T	XP_016880204.1:n.7216-59C>T
XR_934293.2:n.377+1233G>A
XR_934294.2:n.378-597G>A
NM_016239.4:c.7213-59C>T MANE Select	NP_057323.3:n.7213-59C>T