Canonical Allele Identifier: CA107719956

Gene: MMAA

Linked Data

• ClinVar Variation Id: 990262
• ClinVar RCV Id: RCV001278248
• dbSNP Id: rs889048711
• gnomAD v3: 4-145639206-T-C
• gnomAD v4: 4-145639206-T-C
• MyVariant Identifiers: chr4:g.146560358T>C (hg19) ; chr4:g.145639206T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.145639206T>C , CM000666.2:g.145639206T>C	GRCh38
NC_000004.11:g.146560358T>C , CM000666.1:g.146560358T>C	GRCh37
NC_000004.10:g.146779808T>C	NCBI36
NG_007536.1:g.24909T>C
NG_007536.2:g.45165T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000541599.5:c.67T>C	ENSP00000442284.3:p.Cys23Arg
ENST00000647947.1:c.67T>C	ENSP00000496781.1:p.Cys23Arg
ENST00000648388.1:c.67T>C	ENSP00000497046.1:p.Cys23Arg
ENST00000649156.2:c.67T>C MANE Select	ENSP00000497008.1:p.Cys23Arg
ENST00000649173.1:c.67T>C	ENSP00000497871.1:p.Cys23Arg
ENST00000649704.1:c.67T>C	ENSP00000497680.1:p.Cys23Arg
ENST00000679563.1:c.67T>C	ENSP00000506503.1:p.Cys23Arg
ENST00000679930.1:c.67T>C	ENSP00000506293.1:p.Cys23Arg
ENST00000281317.9:c.67T>C	ENSP00000281317.5:p.Cys23Arg
ENST00000506919.1:n.555T>C
ENST00000511969.4:c.67T>C	ENSP00000427422.1:p.Cys23Arg
ENST00000541599.4:c.67T>C	ENSP00000442284.2:p.Cys23Arg
NM_172250.2:c.67T>C	NP_758454.1:p.Cys23Arg
XM_011531684.1:c.67T>C	XP_011529986.1:p.Cys23Arg
XM_011531685.1:c.67T>C	XP_011529987.1:p.Cys23Arg
NM_172250.3:c.67T>C MANE Select	NP_758454.1:p.Cys23Arg
XM_011531684.3:c.67T>C	XP_011529986.1:p.Cys23Arg
XM_011531685.2:c.67T>C	XP_011529987.1:p.Cys23Arg
XM_011531686.2:c.-717T>C	XP_011529988.1:n.-717T>C
NM_001375644.1:c.67T>C	NP_001362573.1:p.Cys23Arg