Canonical Allele Identifier: CA398611889

Gene: MYO15A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18148570T>C , CM000679.2:g.18148570T>C	GRCh38
NC_000017.10:g.18051884T>C , CM000679.1:g.18051884T>C	GRCh37
NC_000017.9:g.17992609T>C	NCBI36
NG_011634.1:g.44865T>C
NG_011634.2:g.44865T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.6764+2T>C MANE Select	ENSP00000495481.1:n.6764+2T>C
ENST00000205890.9:c.6764+2T>C	ENSP00000205890.5:n.6764+2T>C
ENST00000578999.1:n.277-191T>C
ENST00000615845.4:c.6764+2T>C	ENSP00000481642.1:n.6764+2T>C
NM_016239.3:c.6764+2T>C	NP_057323.3:n.6764+2T>C
XM_011523917.1:c.6631+360T>C	XP_011522219.1:n.6631+360T>C
XM_011523921.1:c.6758+2T>C	XP_011522223.1:n.6758+2T>C
XR_934037.1:n.7290+360T>C
XR_934038.1:n.7290+360T>C
XR_934293.1:n.435-964A>G
XR_934295.1:n.254-964A>G
XM_017024714.2:c.6704+2T>C	XP_016880203.1:n.6704+2T>C
XM_017024715.2:c.6767+2T>C	XP_016880204.1:n.6767+2T>C
XR_934293.2:n.378-964A>G
NM_016239.4:c.6764+2T>C MANE Select	NP_057323.3:n.6764+2T>C