Canonical Allele Identifier: CA446831177

Gene: PURA

Linked Data

• MyVariant Identifiers: chr5:g.139494136C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140114551C>T , CM000667.2:g.140114551C>T	GRCh38
NC_000005.9:g.139494136C>T , CM000667.1:g.139494136C>T	GRCh37
NC_000005.8:g.139474320C>T	NCBI36
NG_041813.1:g.5429C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331327.5:c.370C>T MANE Select	ENSP00000332706.3:p.Leu124=
ENST00000651386.1:c.370C>T	ENSP00000499133.1:p.Leu124=
ENST00000331327.4:c.370C>T	ENSP00000332706.3:p.Leu124=
NM_005859.4:c.370C>T	NP_005850.1:p.Leu124=
NM_005859.5:c.370C>T MANE Select	NP_005850.1:p.Leu124=