Canonical Allele Identifier: CA1619235639

Gene: PRRC2A SNORA38

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31623127A= , CM000668.2:g.31623127A=	GRCh38
NC_000006.11:g.31590904A= , CM000668.1:g.31590904A=	GRCh37
NC_000006.10:g.31698883A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376033.3:c.112+226A= (PRRC2A) MANE Select	ENSP00000365201.2:n.112+226A=
ENST00000376007.8:c.112+226A= (PRRC2A)	ENSP00000365175.4:n.112+226A=
ENST00000376033.2:c.112+226A= (PRRC2A)	ENSP00000365201.2:n.112+226A=
ENST00000469577.5:n.136-1134A= (PRRC2A)
NM_004638.3:c.112+226A= (PRRC2A)	NP_004629.3:n.112+226A=
NM_080686.2:c.112+226A= (PRRC2A)	NP_542417.2:n.112+226A=
NR_002971.1:n.49A= (SNORA38)
XM_011514890.1:c.112+226A= (PRRC2A)	XP_011513192.1:n.112+226A=
XM_017011274.1:c.112+226A= (PRRC2A)	XP_016866763.1:n.112+226A=
NM_004638.4:c.112+226A= (PRRC2A) MANE Select	NP_004629.3:n.112+226A=
NM_080686.3:c.112+226A= (PRRC2A)	NP_542417.2:n.112+226A=