Canonical Allele Identifier: CA690194186

Gene: MIP

Linked Data

• dbSNP Id: rs1292077102
• MyVariant Identifiers: chr12:g.56843833_56843834insC (hg19) ; chr12:g.56450049_56450050insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450049_56450050insC , CM000674.2:g.56450049_56450050insC	GRCh38
NC_000012.11:g.56843833_56843834insC , CM000674.1:g.56843833_56843834insC	GRCh37
NC_000012.10:g.55130100_55130101insC	NCBI36
NG_021397.1:g.9602_9603insG
NG_021397.2:g.24117_24118insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1646_*1647insG	ENSP00000497190.1:n.*1646_*1647insG
ENST00000652304.1:c.*1230_*1231insG MANE Select	ENSP00000498622.1:n.*1230_*1231insG
ENST00000257979.4:c.*1230_*1231insG	ENSP00000257979.4:n.*1230_*1231insG
NM_012064.3:c.*1230_*1231insG	NP_036196.1:n.*1230_*1231insG
XM_011538354.1:c.*1230_*1231insG	XP_011536656.1:n.*1230_*1231insG
NM_012064.4:c.*1230_*1231insG MANE Select	NP_036196.1:n.*1230_*1231insG
XM_017019306.1:c.*1230_*1231insG	XP_016874795.1:n.*1230_*1231insG