Canonical Allele Identifier: CA9040381

Gene: MIDN

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1250389G>C , CM000681.2:g.1250389G>C	GRCh38
NC_000019.9:g.1250388G>C , CM000681.1:g.1250388G>C	GRCh37
NC_000019.8:g.1201388G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300952.7:c.93G>C	ENSP00000300952.2:p.Met31Ile
ENST00000591446.7:c.93G>C	ENSP00000467679.1:p.Met31Ile
ENST00000682408.1:c.93G>C MANE Select	ENSP00000507955.1:p.Met31Ile
ENST00000300952.6:c.93G>C	ENSP00000300952.2:p.Met31Ile
ENST00000586757.5:c.93G>C	ENSP00000466895.2:p.Met31Ile
ENST00000591446.6:c.93G>C	ENSP00000467679.1:p.Met31Ile
NM_177401.4:c.93G>C	NP_796375.3:p.Met31Ile
XM_005259671.2:c.93G>C	XP_005259728.1:p.Met31Ile
XM_005259672.2:c.93G>C	XP_005259729.1:p.Met31Ile
XM_005259671.3:c.93G>C	XP_005259728.1:p.Met31Ile
XM_005259672.3:c.93G>C	XP_005259729.1:p.Met31Ile
XM_024451753.1:c.93G>C	XP_024307521.1:p.Met31Ile
XM_024451754.1:c.93G>C	XP_024307522.1:p.Met31Ile
NM_001388306.1:c.93G>C MANE Select	NP_001375235.1:p.Met31Ile
NM_001388307.1:c.93G>C	NP_001375236.1:p.Met31Ile
NM_001388474.1:c.93G>C	NP_001375403.1:p.Met31Ile
NM_177401.5:c.93G>C	NP_796375.3:p.Met31Ile