Canonical Allele Identifier: CA441716112

Gene: MMAA

Linked Data

• MyVariant Identifiers: chr4:g.146560588C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.145639436C>G , CM000666.2:g.145639436C>G	GRCh38
NC_000004.11:g.146560588C>G , CM000666.1:g.146560588C>G	GRCh37
NC_000004.10:g.146780038C>G	NCBI36
NG_007536.1:g.25139C>G
NG_007536.2:g.45395C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000541599.5:c.297C>G	ENSP00000442284.3:p.Ala99=
ENST00000647947.1:c.297C>G	ENSP00000496781.1:p.Ala99=
ENST00000648388.1:c.297C>G	ENSP00000497046.1:p.Ala99=
ENST00000649156.2:c.297C>G MANE Select	ENSP00000497008.1:p.Ala99=
ENST00000649173.1:c.297C>G	ENSP00000497871.1:p.Ala99=
ENST00000649704.1:c.297C>G	ENSP00000497680.1:p.Ala99=
ENST00000679563.1:c.297C>G	ENSP00000506503.1:p.Ala99=
ENST00000679930.1:c.297C>G	ENSP00000506293.1:p.Ala99=
ENST00000281317.9:c.297C>G	ENSP00000281317.5:p.Ala99=
ENST00000506919.1:n.785C>G
ENST00000511969.4:c.297C>G	ENSP00000427422.1:p.Ala99=
ENST00000541599.4:c.297C>G	ENSP00000442284.2:p.Ala99=
NM_172250.2:c.297C>G	NP_758454.1:p.Ala99=
XM_011531684.1:c.297C>G	XP_011529986.1:p.Ala99=
XM_011531685.1:c.297C>G	XP_011529987.1:p.Ala99=
NM_172250.3:c.297C>G MANE Select	NP_758454.1:p.Ala99=
XM_011531684.3:c.297C>G	XP_011529986.1:p.Ala99=
XM_011531685.2:c.297C>G	XP_011529987.1:p.Ala99=
XM_011531686.2:c.-487C>G	XP_011529988.1:n.-487C>G
NM_001375644.1:c.297C>G	NP_001362573.1:p.Ala99=