Canonical Allele Identifier: CA358352799

Gene: MMAA

Linked Data

• dbSNP Id: rs1727719857
• gnomAD v3: 4-145639435-C-T
• gnomAD v4: 4-145639435-C-T
• MyVariant Identifiers: chr4:g.146560587C>T (hg19) ; chr4:g.145639435C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.145639435C>T , CM000666.2:g.145639435C>T	GRCh38
NC_000004.11:g.146560587C>T , CM000666.1:g.146560587C>T	GRCh37
NC_000004.10:g.146780037C>T	NCBI36
NG_007536.1:g.25138C>T
NG_007536.2:g.45394C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000541599.5:c.296C>T	ENSP00000442284.3:p.Ala99Val
ENST00000647947.1:c.296C>T	ENSP00000496781.1:p.Ala99Val
ENST00000648388.1:c.296C>T	ENSP00000497046.1:p.Ala99Val
ENST00000649156.2:c.296C>T MANE Select	ENSP00000497008.1:p.Ala99Val
ENST00000649173.1:c.296C>T	ENSP00000497871.1:p.Ala99Val
ENST00000649704.1:c.296C>T	ENSP00000497680.1:p.Ala99Val
ENST00000679563.1:c.296C>T	ENSP00000506503.1:p.Ala99Val
ENST00000679930.1:c.296C>T	ENSP00000506293.1:p.Ala99Val
ENST00000281317.9:c.296C>T	ENSP00000281317.5:p.Ala99Val
ENST00000506919.1:n.784C>T
ENST00000511969.4:c.296C>T	ENSP00000427422.1:p.Ala99Val
ENST00000541599.4:c.296C>T	ENSP00000442284.2:p.Ala99Val
NM_172250.2:c.296C>T	NP_758454.1:p.Ala99Val
XM_011531684.1:c.296C>T	XP_011529986.1:p.Ala99Val
XM_011531685.1:c.296C>T	XP_011529987.1:p.Ala99Val
NM_172250.3:c.296C>T MANE Select	NP_758454.1:p.Ala99Val
XM_011531684.3:c.296C>T	XP_011529986.1:p.Ala99Val
XM_011531685.2:c.296C>T	XP_011529987.1:p.Ala99Val
XM_011531686.2:c.-488C>T	XP_011529988.1:n.-488C>T
NM_001375644.1:c.296C>T	NP_001362573.1:p.Ala99Val