Canonical Allele Identifier: CA2665748215

Gene: MST1

Linked Data

• gnomAD v4: 3-49683988-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49683988A>G , CM000665.2:g.49683988A>G	GRCh38
NC_000003.11:g.49721421A>G , CM000665.1:g.49721421A>G	GRCh37
NC_000003.10:g.49696425A>G	NCBI36
NG_011438.1:g.14987A>G
NG_016454.1:g.9776T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000449682.3:c.*40T>C MANE Select	ENSP00000414287.2:n.*40T>C
ENST00000448220.5:c.626T>C
ENST00000449682.2:c.*40T>C	ENSP00000414287.2:n.*40T>C
ENST00000479115.5:n.2273T>C
ENST00000488350.6:n.4140T>C
ENST00000492329.5:n.1994T>C
NM_020998.3:c.*40T>C	NP_066278.3:n.*40T>C
XM_006713166.1:c.*40T>C	XP_006713229.1:n.*40T>C
XM_011533730.1:c.*40T>C	XP_011532032.1:n.*40T>C
XM_011533731.1:c.*40T>C	XP_011532033.1:n.*40T>C
XM_011533732.1:c.*40T>C	XP_011532034.1:n.*40T>C
XM_011533733.1:c.*138T>C	XP_011532035.1:n.*138T>C
XR_427270.2:n.3150T>C
XR_427271.1:n.3101T>C
XR_427273.1:n.3006T>C
XR_427274.2:n.3051T>C
XR_940425.1:n.3146T>C
XR_940426.1:n.3186T>C
XR_940427.1:n.3051T>C
NR_146060.1:n.2171T>C
XM_006713166.2:c.*40T>C	XP_006713229.1:n.*40T>C
XM_011533732.2:c.*40T>C	XP_011532034.1:n.*40T>C
XM_017006460.2:c.*40T>C	XP_016861949.1:n.*40T>C
XM_017006461.2:c.*40T>C	XP_016861950.1:n.*40T>C
XM_017006462.2:c.*138T>C	XP_016861951.1:n.*138T>C
XM_017006463.2:c.*138T>C	XP_016861952.1:n.*138T>C
XM_017006464.2:c.*138T>C	XP_016861953.1:n.*138T>C
XR_001740149.2:n.2318T>C
XR_001740150.2:n.2315T>C
XR_001740151.2:n.2358T>C
XR_001740152.2:n.2273T>C
XR_001740153.2:n.2319T>C
XR_002959536.1:n.2273T>C
XR_427273.2:n.2277T>C
XR_940427.2:n.2322T>C
NM_001393581.1:c.*40T>C	NP_001380510.1:n.*40T>C
NM_001393582.1:c.*40T>C	NP_001380511.1:n.*40T>C
NM_001393583.1:c.*40T>C	NP_001380512.1:n.*40T>C
NM_001393584.1:c.*40T>C	NP_001380513.1:n.*40T>C
NM_001393585.1:c.*40T>C	NP_001380514.1:n.*40T>C
NM_020998.4:c.*40T>C MANE Select	NP_066278.3:n.*40T>C
NR_146060.2:n.2882T>C