Canonical Allele Identifier: CA398617255

Gene: MYO15A

Linked Data

• MyVariant Identifiers: chr17:g.18053762C>A (hg19) ; chr17:g.18150448C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18150448C>A , CM000679.2:g.18150448C>A	GRCh38
NC_000017.10:g.18053762C>A , CM000679.1:g.18053762C>A	GRCh37
NC_000017.9:g.17994487C>A	NCBI36
NG_011634.1:g.46743C>A
NG_011634.2:g.46743C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000647165.2:c.7232C>A MANE Select	ENSP00000495481.1:p.Ala2411Asp
ENST00000205890.9:c.7232C>A	ENSP00000205890.5:p.Ala2411Asp
ENST00000615845.4:c.7232C>A	ENSP00000481642.1:p.Ala2411Asp
NM_016239.3:c.7232C>A	NP_057323.3:p.Ala2411Asp
XM_011523917.1:c.6907C>A	XP_011522219.1:p.Pro2303Thr
XM_011523921.1:c.7226C>A	XP_011522223.1:p.Ala2409Asp
XR_934037.1:n.7566C>A
XR_934038.1:n.7518C>A
XR_934293.1:n.434+1155G>T
XR_934294.1:n.435-675G>T
XR_934295.1:n.253+1155G>T
XM_017024714.2:c.7172C>A	XP_016880203.1:p.Ala2391Asp
XM_017024715.2:c.7235C>A	XP_016880204.1:p.Ala2412Asp
XR_934293.2:n.377+1155G>T
XR_934294.2:n.378-675G>T
NM_016239.4:c.7232C>A MANE Select	NP_057323.3:p.Ala2411Asp