Canonical Allele Identifier: CA356792198

Gene: GRXCR1

Linked Data

• MyVariant Identifiers: chr4:g.42964960C>T (hg19) ; chr4:g.42962943C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.42962943C>T , CM000666.2:g.42962943C>T	GRCh38
NC_000004.11:g.42964960C>T , CM000666.1:g.42964960C>T	GRCh37
NC_000004.10:g.42659717C>T	NCBI36
NG_027718.1:g.74678C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399770.3:c.436C>T MANE Select	ENSP00000382670.2:p.Leu146Phe
ENST00000399770.2:c.436C>T	ENSP00000382670.2:p.Leu146Phe
NM_001080476.2:c.436C>T	NP_001073945.1:p.Leu146Phe
XM_011513691.1:c.73C>T	XP_011511993.1:p.Leu25Phe
NM_001080476.3:c.436C>T MANE Select	NP_001073945.1:p.Leu146Phe