Canonical Allele Identifier: CA2636442581

Gene: MYO15A

Linked Data

• gnomAD v4: 17-18138108-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18138108C>T , CM000679.2:g.18138108C>T	GRCh38
NC_000017.10:g.18041422C>T , CM000679.1:g.18041422C>T	GRCh37
NC_000017.9:g.17982147C>T	NCBI36
NG_011634.1:g.34403C>T
NG_011634.2:g.34403C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000646238.1:n.140-7C>T
ENST00000647165.2:c.4876-7C>T MANE Select	ENSP00000495481.1:n.4876-7C>T
ENST00000205890.9:c.4876-7C>T	ENSP00000205890.5:n.4876-7C>T
ENST00000615845.4:c.4876-7C>T	ENSP00000481642.1:n.4876-7C>T
NM_016239.3:c.4876-7C>T	NP_057323.3:n.4876-7C>T
XM_011523917.1:c.4870-7C>T	XP_011522219.1:n.4870-7C>T
XM_011523918.1:c.4870-7C>T	XP_011522220.1:n.4870-7C>T
XM_011523919.1:c.4870-7C>T	XP_011522221.1:n.4870-7C>T
XM_011523920.1:c.4870-7C>T	XP_011522222.1:n.4870-7C>T
XM_011523921.1:c.4870-7C>T	XP_011522223.1:n.4870-7C>T
XR_934037.1:n.5529-7C>T
XR_934038.1:n.5529-7C>T
XR_934039.1:n.5529-7C>T
XM_011523918.2:c.4870-7C>T	XP_011522220.1:n.4870-7C>T
XM_017024714.2:c.4870-7C>T	XP_016880203.1:n.4870-7C>T
XM_017024715.2:c.4879-7C>T	XP_016880204.1:n.4879-7C>T
XM_024450780.1:c.4870-7C>T	XP_024306548.1:n.4870-7C>T
XM_024450781.1:c.4870-7C>T	XP_024306549.1:n.4870-7C>T
XM_024450782.1:c.4870-7C>T	XP_024306550.1:n.4870-7C>T
XR_934039.2:n.5568-7C>T
NM_016239.4:c.4876-7C>T MANE Select	NP_057323.3:n.4876-7C>T