Canonical Allele Identifier: CA2658783108

Gene: MTA3

Linked Data

• gnomAD v4: 2-42754000-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.42754000G>T , CM000664.2:g.42754000G>T	GRCh38
NC_000002.11:g.42981140G>T , CM000664.1:g.42981140G>T	GRCh37
NC_000002.10:g.42834644G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405094.2:c.*601G>T MANE Select	ENSP00000385823.1:n.*601G>T
ENST00000405592.5:c.*601G>T	ENSP00000383973.1:n.*601G>T
ENST00000406652.5:c.*601G>T	ENSP00000384249.1:n.*601G>T
ENST00000409019.5:c.*684G>T	ENSP00000386763.1:n.*684G>T
NM_001282755.1:c.*601G>T	NP_001269684.1:n.*601G>T
NM_001282756.1:c.*601G>T	NP_001269685.1:n.*601G>T
XM_005264456.2:c.*601G>T	XP_005264513.1:n.*601G>T
XM_005264458.2:c.*601G>T	XP_005264515.1:n.*601G>T
XM_005264459.2:c.*601G>T	XP_005264516.1:n.*601G>T
XM_011533006.1:c.*601G>T	XP_011531308.1:n.*601G>T
XR_939697.1:n.1791-29915G>T
XR_939698.1:n.2417G>T
NM_001330442.1:c.*601G>T	NP_001317371.1:n.*601G>T
NM_001330443.1:c.*601G>T	NP_001317372.1:n.*601G>T
NM_001330444.1:c.*601G>T	NP_001317373.1:n.*601G>T
XM_024453019.1:c.*601G>T	XP_024308787.1:n.*601G>T
XR_001738859.2:n.1794-29915G>T
XR_001738860.2:n.2417G>T
XR_939697.3:n.1794-29915G>T
NM_001330442.2:c.*601G>T MANE Select	NP_001317371.1:n.*601G>T
NM_001330443.2:c.*601G>T	NP_001317372.1:n.*601G>T
NM_001330444.2:c.*601G>T	NP_001317373.1:n.*601G>T
NM_001282755.2:c.*601G>T	NP_001269684.1:n.*601G>T
NM_001282756.2:c.*601G>T	NP_001269685.1:n.*601G>T