Canonical Allele Identifier: CA358345140

Gene: MMAA

Linked Data

• MyVariant Identifiers: chr4:g.146576348A>G (hg19) ; chr4:g.145655196A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.145655196A>G , CM000666.2:g.145655196A>G	GRCh38
NC_000004.11:g.146576348A>G , CM000666.1:g.146576348A>G	GRCh37
NC_000004.10:g.146795798A>G	NCBI36
NG_007536.1:g.40899A>G
NG_007536.2:g.61155A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541599.5:c.1019A>G	ENSP00000442284.3:p.Asp340Gly
ENST00000647947.1:c.*803A>G	ENSP00000496781.1:n.*803A>G
ENST00000648388.1:c.1019A>G	ENSP00000497046.1:p.Asp340Gly
ENST00000649156.2:c.1019A>G MANE Select	ENSP00000497008.1:p.Asp340Gly
ENST00000649173.1:c.953A>G	ENSP00000497871.1:p.Asp318Gly
ENST00000649704.1:c.1019A>G	ENSP00000497680.1:p.Asp340Gly
ENST00000679563.1:c.1019A>G	ENSP00000506503.1:p.Asp340Gly
ENST00000679930.1:c.*538A>G	ENSP00000506293.1:n.*538A>G
ENST00000281317.9:c.1019A>G	ENSP00000281317.5:p.Asp340Gly
ENST00000503730.1:n.429A>G
ENST00000511969.4:c.*150A>G	ENSP00000427422.1:n.*150A>G
ENST00000541599.4:c.1019A>G	ENSP00000442284.2:p.Asp340Gly
NM_172250.2:c.1019A>G	NP_758454.1:p.Asp340Gly
XM_011531684.1:c.1019A>G	XP_011529986.1:p.Asp340Gly
XM_011531685.1:c.1019A>G	XP_011529987.1:p.Asp340Gly
XM_011531686.1:c.524A>G	XP_011529988.1:p.Asp175Gly
NM_172250.3:c.1019A>G MANE Select	NP_758454.1:p.Asp340Gly
XM_011531684.3:c.1019A>G	XP_011529986.1:p.Asp340Gly
XM_011531685.2:c.1019A>G	XP_011529987.1:p.Asp340Gly
XM_011531686.2:c.524A>G	XP_011529988.1:p.Asp175Gly
NM_001375644.1:c.1019A>G	NP_001362573.1:p.Asp340Gly