Canonical Allele Identifier: CA384301865

Gene: PYROXD1

Linked Data

• MyVariant Identifiers: chr12:g.21602540T>C (hg19) ; chr12:g.21449606T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.21449606T>C , CM000674.2:g.21449606T>C	GRCh38
NC_000012.11:g.21602540T>C , CM000674.1:g.21602540T>C	GRCh37
NC_000012.10:g.21493807T>C	NCBI36
NG_053196.1:g.17003T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000240651.14:c.329T>C MANE Select	ENSP00000240651.9:p.Leu110Pro
ENST00000240651.13:c.329T>C	ENSP00000240651.9:p.Leu110Pro
ENST00000375266.8:c.*255T>C	ENSP00000364415.4:n.*255T>C
ENST00000538582.5:c.116T>C	ENSP00000438505.1:p.Leu39Pro
ENST00000543476.5:c.329T>C	ENSP00000440192.1:p.Leu110Pro
ENST00000544970.5:c.329T>C	ENSP00000439106.1:p.Leu110Pro
NM_024854.3:c.329T>C	NP_079130.2:p.Leu110Pro
XM_006719153.2:c.329T>C	XP_006719216.1:p.Leu110Pro
XR_242902.3:n.456T>C
NM_001350912.1:c.116T>C	NP_001337841.1:p.Leu39Pro
NM_001350913.1:c.-375T>C	NP_001337842.1:n.-375T>C
NM_024854.4:c.329T>C	NP_079130.2:p.Leu110Pro
XM_006719153.3:c.329T>C	XP_006719216.1:p.Leu110Pro
XR_242902.4:n.430T>C
NM_024854.5:c.329T>C MANE Select	NP_079130.2:p.Leu110Pro
NM_001350913.2:c.-375T>C	NP_001337842.1:n.-375T>C
NM_001350912.2:c.116T>C	NP_001337841.1:p.Leu39Pro