Canonical Allele Identifier: CA502334088

Gene: PYCR1

Linked Data

• MyVariant Identifiers: chr17:g.79891153A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81933277A>G , CM000679.2:g.81933277A>G	GRCh38
NC_000017.10:g.79891153A>G , CM000679.1:g.79891153A>G	GRCh37
NC_000017.9:g.77484444A>G	NCBI36
NG_023032.1:g.8816T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000329875.13:c.897T>C MANE Select	ENSP00000328858.8:p.Ala299=
ENST00000329875.12:c.897T>C	ENSP00000328858.8:p.Ala299=
ENST00000337943.9:c.867+30T>C	ENSP00000336579.5:n.867+30T>C
ENST00000402252.6:c.978T>C	ENSP00000384949.2:p.Ala326=
ENST00000403172.8:c.804T>C	ENSP00000385483.4:p.Ala268=
ENST00000577756.5:c.*79T>C	ENSP00000463352.1:n.*79T>C
ENST00000584848.5:c.601T>C	ENSP00000463342.1:n.601T>C
ENST00000619204.4:c.897T>C	ENSP00000479793.1:p.Ala299=
ENST00000629768.2:c.*79T>C	ENSP00000485679.1:n.*79T>C
NM_001282279.1:c.804T>C	NP_001269208.1:p.Ala268=
NM_001282280.1:c.897T>C	NP_001269209.1:p.Ala299=
NM_001282281.1:c.978T>C	NP_001269210.1:p.Ala326=
NM_006907.3:c.897T>C	NP_008838.2:p.Ala299=
NM_153824.2:c.867+30T>C	NP_722546.1:n.867+30T>C
XM_005256381.1:c.897T>C	XP_005256438.1:p.Ala299=
XM_011523583.1:c.897T>C	XP_011521885.1:p.Ala299=
XM_011523584.1:c.897T>C	XP_011521886.1:p.Ala299=
XM_011523585.1:c.*79T>C	XP_011521887.1:n.*79T>C
NM_001330523.1:c.*79T>C	NP_001317452.1:n.*79T>C
XM_005256381.2:c.897T>C	XP_005256438.1:p.Ala299=
XM_011523583.2:c.897T>C	XP_011521885.1:p.Ala299=
XM_011523584.3:c.897T>C	XP_011521886.1:p.Ala299=
XM_011523585.2:c.*79T>C	XP_011521887.1:n.*79T>C
XM_024450849.1:c.897T>C	XP_024306617.1:p.Ala299=
NM_001282279.2:c.804T>C	NP_001269208.1:p.Ala268=
NM_001282281.2:c.978T>C	NP_001269210.1:p.Ala326=
NM_006907.4:c.897T>C MANE Select	NP_008838.2:p.Ala299=
NM_153824.3:c.867+30T>C	NP_722546.1:n.867+30T>C
NM_001282280.2:c.897T>C	NP_001269209.1:p.Ala299=
NM_001330523.2:c.*79T>C	NP_001317452.1:n.*79T>C