Canonical Allele Identifier: CA364860161

Gene: MRAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.84055382A>G , CM000668.2:g.84055382A>G	GRCh38
NC_000006.11:g.84765101A>G , CM000668.1:g.84765101A>G	GRCh37
NC_000006.10:g.84821820A>G	NCBI36
NG_051944.1:g.26724A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_138409.4:c.64A>G MANE Select	NP_612418.2:p.Thr22Ala
ENST00000257776.5:c.64A>G MANE Select	ENSP00000257776.4:p.Thr22Ala
NM_001346541.1:c.-95A>G	NP_001333470.1:n.-95A>G
NM_001346541.2:c.-95A>G	NP_001333470.1:n.-95A>G
NM_001346542.1:c.64A>G	NP_001333471.1:p.Thr22Ala
NM_001346542.2:c.64A>G	NP_001333471.1:p.Thr22Ala
NM_001346543.1:c.-196A>G	NP_001333472.1:n.-196A>G
NM_001346543.2:c.-196A>G	NP_001333472.1:n.-196A>G
NM_001346544.1:c.64A>G	NP_001333473.1:p.Thr22Ala
NM_001346544.2:c.64A>G	NP_001333473.1:p.Thr22Ala
NM_138409.2:c.64A>G	NP_612418.2:p.Thr22Ala
NM_138409.3:c.64A>G	NP_612418.2:p.Thr22Ala
ENST00000257776.4:c.64A>G	ENSP00000257776.4:p.Thr22Ala
XM_005248644.2:c.64A>G	XP_005248701.1:p.Thr22Ala
XM_005248645.2:c.64A>G	XP_005248702.1:p.Thr22Ala
XM_011535400.1:c.64A>G	XP_011533702.1:p.Thr22Ala
XM_011535401.1:c.64A>G	XP_011533703.1:p.Thr22Ala
XM_011535402.1:c.64A>G	XP_011533704.1:p.Thr22Ala
XM_011535403.1:c.64A>G	XP_011533705.1:p.Thr22Ala
XM_017010220.1:c.64A>G	XP_016865709.1:p.Thr22Ala
XM_017010221.2:c.64A>G	XP_016865710.1:p.Thr22Ala
XM_024446318.1:c.64A>G	XP_024302086.1:p.Thr22Ala