Canonical Allele Identifier: CA8424071

Gene: MYO15A

Linked Data

• dbSNP Id: rs563901690
• ExAC: 17:18041405 G / GCTC
• gnomAD v2: 17-18041405-G-GCTC
• gnomAD v3: 17-18138091-G-GCTC
• gnomAD v4: 17-18138091-G-GCTC
• MyVariant Identifiers: chr17:g.18041405_18041406insCTC (hg19) ; chr17:g.18138091_18138092insCTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18138094_18138096dup , CM000679.2:g.18138094_18138096dup	GRCh38
NC_000017.10:g.18041408_18041410dup , CM000679.1:g.18041408_18041410dup	GRCh37
NC_000017.9:g.17982133_17982135dup	NCBI36
NG_011634.1:g.34389_34391dup
NG_011634.2:g.34389_34391dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000646238.1:n.140-21_140-19dup
ENST00000647165.2:c.4876-21_4876-19dup MANE Select	ENSP00000495481.1:n.4876-21_4876-19dup
ENST00000205890.9:c.4876-21_4876-19dup	ENSP00000205890.5:n.4876-21_4876-19dup
ENST00000615845.4:c.4876-21_4876-19dup	ENSP00000481642.1:n.4876-21_4876-19dup
NM_016239.3:c.4876-21_4876-19dup	NP_057323.3:n.4876-21_4876-19dup
XM_011523917.1:c.4870-21_4870-19dup	XP_011522219.1:n.4870-21_4870-19dup
XM_011523918.1:c.4870-21_4870-19dup	XP_011522220.1:n.4870-21_4870-19dup
XM_011523919.1:c.4870-21_4870-19dup	XP_011522221.1:n.4870-21_4870-19dup
XM_011523920.1:c.4870-21_4870-19dup	XP_011522222.1:n.4870-21_4870-19dup
XM_011523921.1:c.4870-21_4870-19dup	XP_011522223.1:n.4870-21_4870-19dup
XR_934037.1:n.5529-21_5529-19dup
XR_934038.1:n.5529-21_5529-19dup
XR_934039.1:n.5529-21_5529-19dup
XM_011523918.2:c.4870-21_4870-19dup	XP_011522220.1:n.4870-21_4870-19dup
XM_017024714.2:c.4870-21_4870-19dup	XP_016880203.1:n.4870-21_4870-19dup
XM_017024715.2:c.4879-21_4879-19dup	XP_016880204.1:n.4879-21_4879-19dup
XM_024450780.1:c.4870-21_4870-19dup	XP_024306548.1:n.4870-21_4870-19dup
XM_024450781.1:c.4870-21_4870-19dup	XP_024306549.1:n.4870-21_4870-19dup
XM_024450782.1:c.4870-21_4870-19dup	XP_024306550.1:n.4870-21_4870-19dup
XR_934039.2:n.5568-21_5568-19dup
NM_016239.4:c.4876-21_4876-19dup MANE Select	NP_057323.3:n.4876-21_4876-19dup