Canonical Allele Identifier: CA2843303831

Gene: MTARC2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.220756007A>T , CM000663.2:g.220756007A>T	GRCh38
NC_000001.10:g.220929349A>T , CM000663.1:g.220929349A>T	GRCh37
NC_000001.9:g.218995972A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366913.8:c.446+887A>T MANE Select	ENSP00000355880.3:n.446+887A>T
ENST00000359316.6:c.446+887A>T	ENSP00000352266.2:n.446+887A>T
ENST00000366913.7:c.446+887A>T	ENSP00000355880.3:n.446+887A>T
ENST00000425560.1:c.149+887A>T	ENSP00000416442.1:n.149+887A>T
NM_017898.3:c.446+887A>T	NP_060368.2:n.446+887A>T
XM_005273168.3:c.446+887A>T	XP_005273225.1:n.446+887A>T
XM_006711407.2:c.-525A>T	XP_006711470.1:n.-525A>T
XM_011509683.1:c.-110+781A>T	XP_011507985.1:n.-110+781A>T
XM_011509684.1:c.176+887A>T	XP_011507986.1:n.176+887A>T
XR_247029.3:n.1476+887A>T
NM_001317338.1:c.446+887A>T	NP_001304267.1:n.446+887A>T
NM_001331042.1:c.446+887A>T	NP_001317971.1:n.446+887A>T
NM_017898.4:c.446+887A>T	NP_060368.2:n.446+887A>T
XR_247029.5:n.1561+887A>T
NM_017898.5:c.446+887A>T MANE Select	NP_060368.2:n.446+887A>T
NM_001317338.2:c.446+887A>T	NP_001304267.1:n.446+887A>T
NM_001331042.2:c.446+887A>T	NP_001317971.1:n.446+887A>T