Canonical Allele Identifier: CA3095098

Gene: MMAA

Linked Data

• ClinVar Variation Id: 990260
• ClinVar RCV Id: RCV001278246 ; RCV003963171
• dbSNP Id: rs374109118
• ExAC: 4:146560288 G / A
• gnomAD v2: 4-146560288-G-A
• gnomAD v3: 4-145639136-G-A
• gnomAD v4: 4-145639136-G-A
• MyVariant Identifiers: chr4:g.146560288G>A (hg19) ; chr4:g.145639136G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.145639136G>A , CM000666.2:g.145639136G>A	GRCh38
NC_000004.11:g.146560288G>A , CM000666.1:g.146560288G>A	GRCh37
NC_000004.10:g.146779738G>A	NCBI36
NG_007536.1:g.24839G>A
NG_007536.2:g.45095G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541599.5:c.-4G>A	ENSP00000442284.3:n.-4G>A
ENST00000647947.1:c.-4G>A	ENSP00000496781.1:n.-4G>A
ENST00000648388.1:c.-4G>A	ENSP00000497046.1:n.-4G>A
ENST00000649156.2:c.-4G>A MANE Select	ENSP00000497008.1:n.-4G>A
ENST00000649173.1:c.-4G>A	ENSP00000497871.1:n.-4G>A
ENST00000649704.1:c.-4G>A	ENSP00000497680.1:n.-4G>A
ENST00000679563.1:c.-4G>A	ENSP00000506503.1:n.-4G>A
ENST00000679930.1:c.-4G>A	ENSP00000506293.1:n.-4G>A
ENST00000281317.9:c.-4G>A	ENSP00000281317.5:n.-4G>A
ENST00000506919.1:n.485G>A
ENST00000511969.4:c.-4G>A	ENSP00000427422.1:n.-4G>A
ENST00000541599.4:c.-4G>A	ENSP00000442284.2:n.-4G>A
NM_172250.2:c.-4G>A	NP_758454.1:n.-4G>A
XM_011531684.1:c.-4G>A	XP_011529986.1:n.-4G>A
XM_011531685.1:c.-4G>A	XP_011529987.1:n.-4G>A
NM_172250.3:c.-4G>A MANE Select	NP_758454.1:n.-4G>A
XM_011531684.3:c.-4G>A	XP_011529986.1:n.-4G>A
XM_011531685.2:c.-4G>A	XP_011529987.1:n.-4G>A
XM_011531686.2:c.-787G>A	XP_011529988.1:n.-787G>A
NM_001375644.1:c.-4G>A	NP_001362573.1:n.-4G>A