Canonical Allele Identifier: CA15391123

Gene: REEP5 SRP19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112890958C>T , CM000667.2:g.112890958C>T	GRCh38
NC_000005.9:g.112226655C>T , CM000667.1:g.112226655C>T	GRCh37
NC_000005.8:g.112254554C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005669.5:c.352-3775G>A (REEP5) MANE Select	NP_005660.4:n.352-3775G>A
ENST00000379638.9:c.352-3775G>A (REEP5) MANE Select	ENSP00000368959.4:n.352-3775G>A
NM_001204199.1:c.302-645C>T (SRP19)	NP_001191128.1:n.302-645C>T
NM_001204199.2:c.302-645C>T (SRP19)	NP_001191128.1:n.302-645C>T
NM_005669.4:c.352-3775G>A (REEP5)	NP_005660.4:n.352-3775G>A
ENST00000261482.8:c.325-3775G>A (REEP5)	ENSP00000261482.4:n.325-3775G>A
ENST00000379638.8:c.352-3775G>A (REEP5)	ENSP00000368959.4:n.352-3775G>A
ENST00000391338.3:c.302-645C>T (SRP19)	ENSP00000375133.2:n.302-645C>T
ENST00000474542.2:n.482-3775G>A (REEP5)
ENST00000497856.6:n.859+1492G>A (REEP5)
ENST00000503445.5:n.472-645C>T
ENST00000504247.1:c.213-3775G>A (REEP5)	ENSP00000421881.1:n.213-3775G>A
ENST00000506997.1:c.*81-645C>T	ENSP00000424153.1:n.*81-645C>T
ENST00000506997.2:c.*81-645C>T (SRP19)	ENSP00000424153.1:n.*81-645C>T
ENST00000509024.2:n.352-645C>T
ENST00000511865.6:c.759+1492G>A (REEP5)
ENST00000512790.5:n.374-645C>T
ENST00000513339.5:c.351+11422G>A (REEP5)	ENSP00000425901.1:n.351+11422G>A
XM_017009844.2:c.352-3775G>A (REEP5)	XP_016865333.1:n.352-3775G>A