Canonical Allele Identifier: CA9040918

Gene: MIDN

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1255692C>T , CM000681.2:g.1255692C>T	GRCh38
NC_000019.9:g.1255691C>T , CM000681.1:g.1255691C>T	GRCh37
NC_000019.8:g.1206691C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300952.7:c.1127C>T	ENSP00000300952.2:p.Pro376Leu
ENST00000591446.7:c.1127C>T	ENSP00000467679.1:p.Pro376Leu
ENST00000682408.1:c.1256C>T MANE Select	ENSP00000507955.1:p.Pro419Leu
ENST00000300952.6:c.1127C>T	ENSP00000300952.2:p.Pro376Leu
ENST00000591446.6:c.1127C>T	ENSP00000467679.1:p.Pro376Leu
NM_177401.4:c.1127C>T	NP_796375.3:p.Pro376Leu
XM_005259671.2:c.1256C>T	XP_005259728.1:p.Pro419Leu
XM_005259672.2:c.1253C>T	XP_005259729.1:p.Pro418Leu
XM_005259671.3:c.1256C>T	XP_005259728.1:p.Pro419Leu
XM_005259672.3:c.1253C>T	XP_005259729.1:p.Pro418Leu
XM_024451753.1:c.1616C>T	XP_024307521.1:p.Pro539Leu
XM_024451754.1:c.1487C>T	XP_024307522.1:p.Pro496Leu
NM_001388306.1:c.1256C>T MANE Select	NP_001375235.1:p.Pro419Leu
NM_001388307.1:c.1124C>T	NP_001375236.1:p.Pro375Leu
NM_001388474.1:c.1127C>T	NP_001375403.1:p.Pro376Leu
NM_177401.5:c.1127C>T	NP_796375.3:p.Pro376Leu