Canonical Allele Identifier: CA398625644

Gene: MYO15A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18154714G>C , CM000679.2:g.18154714G>C	GRCh38
NC_000017.10:g.18058028G>C , CM000679.1:g.18058028G>C	GRCh37
NC_000017.9:g.17998753G>C	NCBI36
NG_011634.1:g.51009G>C
NG_011634.2:g.51009G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642418.1:n.30G>C
ENST00000644795.1:c.-26G>C	ENSP00000495720.1:n.-26G>C
ENST00000646782.1:n.338G>C
ENST00000647165.2:c.8183G>C MANE Select	ENSP00000495481.1:p.Arg2728Pro
ENST00000651214.1:n.329G>C
ENST00000205890.9:c.8183G>C	ENSP00000205890.5:p.Arg2728Pro
ENST00000418233.7:c.-26G>C	ENSP00000408800.3:n.-26G>C
ENST00000445289.6:n.137+524G>C
ENST00000536811.5:n.138-396G>C
ENST00000585180.1:c.-26G>C	ENSP00000464462.1:n.-26G>C
ENST00000615845.4:c.8183G>C	ENSP00000481642.1:p.Arg2728Pro
NM_016239.3:c.8183G>C	NP_057323.3:p.Arg2728Pro
XM_011523921.1:c.8177G>C	XP_011522223.1:p.Arg2726Pro
XM_017024714.2:c.8123G>C	XP_016880203.1:p.Arg2708Pro
XM_017024715.2:c.8186G>C	XP_016880204.1:p.Arg2729Pro
XR_001752809.1:n.95C>G
XR_001752810.1:n.95C>G
NM_016239.4:c.8183G>C MANE Select	NP_057323.3:p.Arg2728Pro