Canonical Allele Identifier: CA2841146539

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394957_40394958insT , CM000681.2:g.40394957_40394958insT	GRCh38
NC_000019.9:g.40900864_40900865insT , CM000681.1:g.40900864_40900865insT	GRCh37
NC_000019.8:g.45592704_45592705insT	NCBI36
NG_007979.1:g.23407_23408insA , LRG_265:g.23407_23408insA
NG_051224.1:g.264_265insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3394_3395insA MANE Select	ENSP00000326018.6:p.Gly1132GlufsTer6
ENST00000673881.1:c.2977_2978insA	ENSP00000501070.1:p.Gly993GlufsTer6
ENST00000674005.2:c.3679_3680insA	ENSP00000501261.1:p.Gly1227GlufsTer6
ENST00000674773.1:c.2977_2978insA	ENSP00000502579.1:p.Gly993GlufsTer6
ENST00000675517.1:c.3269_3270insA
ENST00000676076.1:c.3255_3256insA
ENST00000676260.1:c.3356_3357insA
ENST00000676316.1:c.3281_3282insA
ENST00000291825.11:c.*3599_*3600insA	ENSP00000291825.6:n.*3599_*3600insA
ENST00000324001.7:c.3394_3395insA	ENSP00000326018.6:p.Gly1132GlufsTer6
NM_020956.2:c.*3599_*3600insA , LRG_265t1:c.*3599_*3600insA	NP_066007.1:n.*3599_*3600insA
NM_181882.2:c.3394_3395insA , LRG_265t2:c.3394_3395insA	NP_870998.2:p.Gly1132GlufsTer6
XM_011527171.1:c.3394_3395insA	XP_011525473.1:p.Gly1132GlufsTer6
XM_011527171.2:c.3394_3395insA	XP_011525473.1:p.Gly1132GlufsTer6
XM_017027046.1:c.3292_3293insA	XP_016882535.1:p.Gly1098GlufsTer6
XM_017027047.1:c.3292_3293insA	XP_016882536.1:p.Gly1098GlufsTer6
NM_181882.3:c.3394_3395insA MANE Select	NP_870998.2:p.Gly1132GlufsTer6