Canonical Allele Identifier: CA2576190679

Gene: MYO15A

Linked Data

• gnomAD v4: 17-18150345-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.18150345A>C , CM000679.2:g.18150345A>C	GRCh38
NC_000017.10:g.18053659A>C , CM000679.1:g.18053659A>C	GRCh37
NC_000017.9:g.17994384A>C	NCBI36
NG_011634.1:g.46640A>C
NG_011634.2:g.46640A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000647165.2:c.7213-84A>C MANE Select	ENSP00000495481.1:n.7213-84A>C
ENST00000205890.9:c.7213-84A>C	ENSP00000205890.5:n.7213-84A>C
ENST00000615845.4:c.7213-84A>C	ENSP00000481642.1:n.7213-84A>C
NM_016239.3:c.7213-84A>C	NP_057323.3:n.7213-84A>C
XM_011523917.1:c.6888-84A>C	XP_011522219.1:n.6888-84A>C
XM_011523921.1:c.7207-84A>C	XP_011522223.1:n.7207-84A>C
XR_934037.1:n.7547-84A>C
XR_934038.1:n.7499-84A>C
XR_934293.1:n.434+1258T>G
XR_934294.1:n.435-572T>G
XR_934295.1:n.253+1258T>G
XM_017024714.2:c.7153-84A>C	XP_016880203.1:n.7153-84A>C
XM_017024715.2:c.7216-84A>C	XP_016880204.1:n.7216-84A>C
XR_934293.2:n.377+1258T>G
XR_934294.2:n.378-572T>G
NM_016239.4:c.7213-84A>C MANE Select	NP_057323.3:n.7213-84A>C