Canonical Allele Identifier: CA2581390120

Gene: PRMT1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49685899G>T , CM000681.2:g.49685899G>T	GRCh38
NC_000019.9:g.50189156G>T , CM000681.1:g.50189156G>T	GRCh37
NC_000019.8:g.54880968G>T	NCBI36
NG_031846.1:g.13748G>T
NG_050570.1:g.22G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001536.6:c.760-194G>T MANE Select	NP_001527.3:n.760-194G>T
ENST00000454376.7:c.760-194G>T MANE Select	ENSP00000406162.2:n.760-194G>T
NM_001207042.2:c.502-194G>T	NP_001193971.1:n.502-194G>T
NM_001207042.3:c.502-194G>T	NP_001193971.1:n.502-194G>T
NM_001536.5:c.760-194G>T	NP_001527.3:n.760-194G>T
NM_198318.4:c.706-194G>T	NP_938074.2:n.706-194G>T
NM_198318.5:c.706-194G>T	NP_938074.2:n.706-194G>T
NR_033397.4:n.1007-194G>T
NR_033397.5:n.888-194G>T
ENST00000391851.8:c.706-194G>T	ENSP00000375724.4:n.706-194G>T
ENST00000454376.6:c.760-194G>T	ENSP00000406162.2:n.760-194G>T
ENST00000528126.1:n.176G>T
ENST00000530361.5:n.336-194G>T
ENST00000532489.5:c.622-194G>T	ENSP00000433556.1:n.622-194G>T
ENST00000610806.4:c.502-194G>T	ENSP00000484505.1:n.502-194G>T
XM_005258842.1:c.673-194G>T	XP_005258899.1:n.673-194G>T
XM_005258844.3:c.*667G>T	XP_005258901.1:n.*667G>T
XM_011526892.1:c.673-194G>T	XP_011525194.1:n.673-194G>T
XM_017026734.1:c.688-194G>T	XP_016882223.1:n.688-194G>T
XM_017026735.1:c.688-194G>T	XP_016882224.1:n.688-194G>T
XM_017026736.1:c.673-194G>T	XP_016882225.1:n.673-194G>T