Canonical Allele Identifier: CA2658783120

Gene: MTA3

Linked Data

• gnomAD v4: 2-42754019-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.42754020del , CM000664.2:g.42754020del	GRCh38
NC_000002.11:g.42981160del , CM000664.1:g.42981160del	GRCh37
NC_000002.10:g.42834664del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405094.2:c.*621del MANE Select	ENSP00000385823.1:n.*621del
ENST00000405592.5:c.*621del	ENSP00000383973.1:n.*621del
ENST00000406652.5:c.*621del	ENSP00000384249.1:n.*621del
ENST00000409019.5:c.*704del	ENSP00000386763.1:n.*704del
NM_001282755.1:c.*621del	NP_001269684.1:n.*621del
NM_001282756.1:c.*621del	NP_001269685.1:n.*621del
XM_005264456.2:c.*621del	XP_005264513.1:n.*621del
XM_005264458.2:c.*621del	XP_005264515.1:n.*621del
XM_005264459.2:c.*621del	XP_005264516.1:n.*621del
XM_011533006.1:c.*621del	XP_011531308.1:n.*621del
XR_939697.1:n.1791-29895del
XR_939698.1:n.2437del
NM_001330442.1:c.*621del	NP_001317371.1:n.*621del
NM_001330443.1:c.*621del	NP_001317372.1:n.*621del
NM_001330444.1:c.*621del	NP_001317373.1:n.*621del
XM_024453019.1:c.*621del	XP_024308787.1:n.*621del
XR_001738859.2:n.1794-29895del
XR_001738860.2:n.2437del
XR_939697.3:n.1794-29895del
NM_001330442.2:c.*621del MANE Select	NP_001317371.1:n.*621del
NM_001330443.2:c.*621del	NP_001317372.1:n.*621del
NM_001330444.2:c.*621del	NP_001317373.1:n.*621del
NM_001282755.2:c.*621del	NP_001269684.1:n.*621del
NM_001282756.2:c.*621del	NP_001269685.1:n.*621del