Canonical Allele Identifier: CA6913450

Gene: MIPEP PCOTH

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23889306T>G , CM000675.2:g.23889306T>G	GRCh38
NC_000013.10:g.24463445T>G , CM000675.1:g.24463445T>G	GRCh37
NC_000013.9:g.23361445T>G	NCBI36
NG_052977.1:g.5143A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382172.4:c.15A>C (MIPEP) MANE Select	ENSP00000371607.3:p.Gly5=
ENST00000382172.3:c.15A>C (MIPEP)	ENSP00000371607.3:p.Gly5=
ENST00000469167.1:n.93A>C (MIPEP)
NM_001014442.2:c.-186+295T>G (PCOTH)	NP_001014442.2:n.-186+295T>G
NM_005932.3:c.15A>C (MIPEP)	NP_005923.2:p.Gly5=
XM_011535098.1:c.15A>C (MIPEP)	XP_011533400.1:p.Gly5=
NM_001014442.3:c.-186+295T>G (PCOTH)	NP_001014442.2:n.-186+295T>G
XM_011535098.3:c.15A>C (MIPEP)	XP_011533400.1:p.Gly5=
NM_005932.4:c.15A>C (MIPEP) MANE Select	NP_005923.3:p.Gly5=
NM_001014442.4:c.-186+295T>G (PCOTH)	NP_001014442.2:n.-186+295T>G
NR_172510.1:n.144+295T>G (PCOTH)