Canonical Allele Identifier: CA2636449760

Gene: MYO15A

Linked Data

• ClinVar Variation Id: 2766674
• ClinVar RCV Id: RCV003580389
• gnomAD v4: 17-18154200-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18154200T>C , CM000679.2:g.18154200T>C	GRCh38
NC_000017.10:g.18057514T>C , CM000679.1:g.18057514T>C	GRCh37
NC_000017.9:g.17998239T>C	NCBI36
NG_011634.1:g.50495T>C
NG_011634.2:g.50495T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644795.1:c.-61+10T>C	ENSP00000495720.1:n.-61+10T>C
ENST00000646782.1:n.303+10T>C
ENST00000647165.2:c.8148+10T>C MANE Select	ENSP00000495481.1:n.8148+10T>C
ENST00000651214.1:n.294+10T>C
ENST00000205890.9:c.8148+10T>C	ENSP00000205890.5:n.8148+10T>C
ENST00000418233.7:c.-61+10T>C	ENSP00000408800.3:n.-61+10T>C
ENST00000445289.6:n.137+10T>C
ENST00000536811.5:n.137+10T>C
ENST00000585180.1:c.-61+10T>C	ENSP00000464462.1:n.-61+10T>C
ENST00000615845.4:c.8148+10T>C	ENSP00000481642.1:n.8148+10T>C
NM_016239.3:c.8148+10T>C	NP_057323.3:n.8148+10T>C
XM_011523921.1:c.8142+10T>C	XP_011522223.1:n.8142+10T>C
XM_017024714.2:c.8088+10T>C	XP_016880203.1:n.8088+10T>C
XM_017024715.2:c.8151+10T>C	XP_016880204.1:n.8151+10T>C
XR_001752809.1:n.237A>G
XR_001752810.1:n.237A>G
NM_016239.4:c.8148+10T>C MANE Select	NP_057323.3:n.8148+10T>C