Canonical Allele Identifier: CA141972694

Gene: MRAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.84055376G>C , CM000668.2:g.84055376G>C	GRCh38
NC_000006.11:g.84765095G>C , CM000668.1:g.84765095G>C	GRCh37
NC_000006.10:g.84821814G>C	NCBI36
NG_051944.1:g.26718G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_138409.4:c.58G>C MANE Select	NP_612418.2:p.Asp20His
ENST00000257776.5:c.58G>C MANE Select	ENSP00000257776.4:p.Asp20His
NM_001346541.1:c.-101G>C	NP_001333470.1:n.-101G>C
NM_001346541.2:c.-101G>C	NP_001333470.1:n.-101G>C
NM_001346542.1:c.58G>C	NP_001333471.1:p.Asp20His
NM_001346542.2:c.58G>C	NP_001333471.1:p.Asp20His
NM_001346543.1:c.-202G>C	NP_001333472.1:n.-202G>C
NM_001346543.2:c.-202G>C	NP_001333472.1:n.-202G>C
NM_001346544.1:c.58G>C	NP_001333473.1:p.Asp20His
NM_001346544.2:c.58G>C	NP_001333473.1:p.Asp20His
NM_138409.2:c.58G>C	NP_612418.2:p.Asp20His
NM_138409.3:c.58G>C	NP_612418.2:p.Asp20His
ENST00000257776.4:c.58G>C	ENSP00000257776.4:p.Asp20His
XM_005248644.2:c.58G>C	XP_005248701.1:p.Asp20His
XM_005248645.2:c.58G>C	XP_005248702.1:p.Asp20His
XM_011535400.1:c.58G>C	XP_011533702.1:p.Asp20His
XM_011535401.1:c.58G>C	XP_011533703.1:p.Asp20His
XM_011535402.1:c.58G>C	XP_011533704.1:p.Asp20His
XM_011535403.1:c.58G>C	XP_011533705.1:p.Asp20His
XM_017010220.1:c.58G>C	XP_016865709.1:p.Asp20His
XM_017010221.2:c.58G>C	XP_016865710.1:p.Asp20His
XM_024446318.1:c.58G>C	XP_024302086.1:p.Asp20His