Canonical Allele Identifier: CA2636439818

Gene: MYO15A

Linked Data

• gnomAD v4: 17-18150368-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18150369dup , CM000679.2:g.18150369dup	GRCh38
NC_000017.10:g.18053683dup , CM000679.1:g.18053683dup	GRCh37
NC_000017.9:g.17994408dup	NCBI36
NG_011634.1:g.46664dup
NG_011634.2:g.46664dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000647165.2:c.7213-60dup MANE Select	ENSP00000495481.1:n.7213-60dup
ENST00000205890.9:c.7213-60dup	ENSP00000205890.5:n.7213-60dup
ENST00000615845.4:c.7213-60dup	ENSP00000481642.1:n.7213-60dup
NM_016239.3:c.7213-60dup	NP_057323.3:n.7213-60dup
XM_011523917.1:c.6888-60dup	XP_011522219.1:n.6888-60dup
XM_011523921.1:c.7207-60dup	XP_011522223.1:n.7207-60dup
XR_934037.1:n.7547-60dup
XR_934038.1:n.7499-60dup
XR_934293.1:n.434+1234dup
XR_934294.1:n.435-596dup
XR_934295.1:n.253+1234dup
XM_017024714.2:c.7153-60dup	XP_016880203.1:n.7153-60dup
XM_017024715.2:c.7216-60dup	XP_016880204.1:n.7216-60dup
XR_934293.2:n.377+1234dup
XR_934294.2:n.378-596dup
NM_016239.4:c.7213-60dup MANE Select	NP_057323.3:n.7213-60dup