Canonical Allele Identifier: CA405902081

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40407931A>G , CM000681.2:g.40407931A>G	GRCh38
NC_000019.9:g.40913838A>G , CM000681.1:g.40913838A>G	GRCh37
NC_000019.8:g.45605678A>G	NCBI36
NG_007979.1:g.10434T>C , LRG_265:g.10434T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.2T>C MANE Select	NP_870998.2:p.Met1Thr
ENST00000324001.8:c.2T>C MANE Select	ENSP00000326018.6:p.Met1Thr
NM_020956.2:c.2T>C , LRG_265t1:c.2T>C	NP_066007.1:p.Met1Thr
NM_181882.2:c.2T>C , LRG_265t2:c.2T>C	NP_870998.2:p.Met1Thr
ENST00000291825.11:c.2T>C	ENSP00000291825.6:p.Met1Thr
ENST00000324001.7:c.2T>C	ENSP00000326018.6:p.Met1Thr
ENST00000599513.1:n.187T>C
ENST00000674005.2:c.287T>C	ENSP00000501261.1:p.Met96Thr
ENST00000674781.1:n.101T>C
ENST00000674912.1:n.101T>C
ENST00000675484.1:c.145T>C
ENST00000675541.1:n.101T>C
ENST00000676344.1:n.101T>C
XM_011527171.1:c.2T>C	XP_011525473.1:p.Met1Thr
XM_011527171.2:c.2T>C	XP_011525473.1:p.Met1Thr