Canonical Allele Identifier: CA405894056

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40900893C>G (hg19) ; chr19:g.40394986C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394986C>G , CM000681.2:g.40394986C>G	GRCh38
NC_000019.9:g.40900893C>G , CM000681.1:g.40900893C>G	GRCh37
NC_000019.8:g.45592733C>G	NCBI36
NG_007979.1:g.23379G>C , LRG_265:g.23379G>C
NG_051224.1:g.236G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3366G>C MANE Select	ENSP00000326018.6:p.Gln1122His
ENST00000673881.1:c.2949G>C	ENSP00000501070.1:p.Gln983His
ENST00000674005.2:c.3651G>C	ENSP00000501261.1:p.Gln1217His
ENST00000674773.1:c.2949G>C	ENSP00000502579.1:p.Gln983His
ENST00000675517.1:c.3241G>C
ENST00000676076.1:c.3227G>C
ENST00000676260.1:c.3328G>C
ENST00000676316.1:c.3253G>C
ENST00000291825.11:c.*3571G>C	ENSP00000291825.6:n.*3571G>C
ENST00000324001.7:c.3366G>C	ENSP00000326018.6:p.Gln1122His
NM_020956.2:c.*3571G>C , LRG_265t1:c.*3571G>C	NP_066007.1:n.*3571G>C
NM_181882.2:c.3366G>C , LRG_265t2:c.3366G>C	NP_870998.2:p.Gln1122His
XM_011527171.1:c.3366G>C	XP_011525473.1:p.Gln1122His
XM_011527171.2:c.3366G>C	XP_011525473.1:p.Gln1122His
XM_017027046.1:c.3264G>C	XP_016882535.1:p.Gln1088His
XM_017027047.1:c.3264G>C	XP_016882536.1:p.Gln1088His
NM_181882.3:c.3366G>C MANE Select	NP_870998.2:p.Gln1122His