Canonical Allele Identifier: CA2278748846

Gene: PYCR1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81933168_81933173delinsCAAGAG , CM000679.2:g.81933168_81933173delinsCAAGAG	GRCh38
NC_000017.10:g.79891044_79891049delinsCAAGAG , CM000679.1:g.79891044_79891049delinsCAAGAG	GRCh37
NC_000017.9:g.77484335_77484340delinsCAAGAG	NCBI36
NG_023032.1:g.8920_8925delinsCTCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329875.13:c.*41_*46delinsCTCTTG MANE Select	ENSP00000328858.8:n.*41_*46delinsCTCTTG
ENST00000329875.12:c.*41_*46delinsCTCTTG	ENSP00000328858.8:n.*41_*46delinsCTCTTG
ENST00000337943.9:c.867+134_867+139delinsCTCTTG	ENSP00000336579.5:n.867+134_867+139delinsCTCTTG
ENST00000402252.6:c.*41_*46delinsCTCTTG	ENSP00000384949.2:n.*41_*46delinsCTCTTG
ENST00000403172.8:c.*41_*46delinsCTCTTG	ENSP00000385483.4:n.*41_*46delinsCTCTTG
ENST00000577756.5:c.*183_*188delinsCTCTTG	ENSP00000463352.1:n.*183_*188delinsCTCTTG
ENST00000584848.5:c.705_710delinsCTCTTG	ENSP00000463342.1:n.705_710delinsCTCTTG
ENST00000619204.4:c.*41_*46delinsCTCTTG	ENSP00000479793.1:n.*41_*46delinsCTCTTG
ENST00000629768.2:c.*183_*188delinsCTCTTG	ENSP00000485679.1:n.*183_*188delinsCTCTTG
NM_001282279.1:c.*41_*46delinsCTCTTG	NP_001269208.1:n.*41_*46delinsCTCTTG
NM_001282280.1:c.*41_*46delinsCTCTTG	NP_001269209.1:n.*41_*46delinsCTCTTG
NM_001282281.1:c.*41_*46delinsCTCTTG	NP_001269210.1:n.*41_*46delinsCTCTTG
NM_006907.3:c.*41_*46delinsCTCTTG	NP_008838.2:n.*41_*46delinsCTCTTG
NM_153824.2:c.867+134_867+139delinsCTCTTG	NP_722546.1:n.867+134_867+139delinsCTCTTG
XM_005256381.1:c.*41_*46delinsCTCTTG	XP_005256438.1:n.*41_*46delinsCTCTTG
XM_011523583.1:c.*41_*46delinsCTCTTG	XP_011521885.1:n.*41_*46delinsCTCTTG
XM_011523584.1:c.*41_*46delinsCTCTTG	XP_011521886.1:n.*41_*46delinsCTCTTG
XM_011523585.1:c.*183_*188delinsCTCTTG	XP_011521887.1:n.*183_*188delinsCTCTTG
NM_001330523.1:c.*183_*188delinsCTCTTG	NP_001317452.1:n.*183_*188delinsCTCTTG
XM_005256381.2:c.*41_*46delinsCTCTTG	XP_005256438.1:n.*41_*46delinsCTCTTG
XM_011523583.2:c.*41_*46delinsCTCTTG	XP_011521885.1:n.*41_*46delinsCTCTTG
XM_011523584.3:c.*41_*46delinsCTCTTG	XP_011521886.1:n.*41_*46delinsCTCTTG
XM_011523585.2:c.*183_*188delinsCTCTTG	XP_011521887.1:n.*183_*188delinsCTCTTG
XM_024450849.1:c.*41_*46delinsCTCTTG	XP_024306617.1:n.*41_*46delinsCTCTTG
NM_001282279.2:c.*41_*46delinsCTCTTG	NP_001269208.1:n.*41_*46delinsCTCTTG
NM_001282281.2:c.*41_*46delinsCTCTTG	NP_001269210.1:n.*41_*46delinsCTCTTG
NM_006907.4:c.*41_*46delinsCTCTTG MANE Select	NP_008838.2:n.*41_*46delinsCTCTTG
NM_153824.3:c.867+134_867+139delinsCTCTTG	NP_722546.1:n.867+134_867+139delinsCTCTTG
NM_001282280.2:c.*41_*46delinsCTCTTG	NP_001269209.1:n.*41_*46delinsCTCTTG
NM_001330523.2:c.*183_*188delinsCTCTTG	NP_001317452.1:n.*183_*188delinsCTCTTG