Canonical Allele Identifier: CA234076806

Gene: PYROXD1

Linked Data

• dbSNP Id: rs377212635
• MyVariant Identifiers: chr12:g.21602529A>T (hg19) ; chr12:g.21449595A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21449595A>T , CM000674.2:g.21449595A>T	GRCh38
NC_000012.11:g.21602529A>T , CM000674.1:g.21602529A>T	GRCh37
NC_000012.10:g.21493796A>T	NCBI36
NG_053196.1:g.16992A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000240651.14:c.318A>T MANE Select	ENSP00000240651.9:p.Val106=
ENST00000240651.13:c.318A>T	ENSP00000240651.9:p.Val106=
ENST00000375266.8:c.*244A>T	ENSP00000364415.4:n.*244A>T
ENST00000538582.5:c.105A>T	ENSP00000438505.1:p.Val35=
ENST00000543476.5:c.318A>T	ENSP00000440192.1:p.Val106=
ENST00000544970.5:c.318A>T	ENSP00000439106.1:p.Val106=
NM_024854.3:c.318A>T	NP_079130.2:p.Val106=
XM_006719153.2:c.318A>T	XP_006719216.1:p.Val106=
XR_242902.3:n.445A>T
NM_001350912.1:c.105A>T	NP_001337841.1:p.Val35=
NM_001350913.1:c.-386A>T	NP_001337842.1:n.-386A>T
NM_024854.4:c.318A>T	NP_079130.2:p.Val106=
XM_006719153.3:c.318A>T	XP_006719216.1:p.Val106=
XR_242902.4:n.419A>T
NM_024854.5:c.318A>T MANE Select	NP_079130.2:p.Val106=
NM_001350913.2:c.-386A>T	NP_001337842.1:n.-386A>T
NM_001350912.2:c.105A>T	NP_001337841.1:p.Val35=