Canonical Allele Identifier: CA2038370046

Gene: MIP

Linked Data

• dbSNP Id: rs1868551705

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450338G>C , CM000674.2:g.56450338G>C	GRCh38
NC_000012.11:g.56844122G>C , CM000674.1:g.56844122G>C	GRCh37
NC_000012.10:g.55130389G>C	NCBI36
NG_021397.1:g.9314C>G
NG_021397.2:g.23829C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1358C>G	ENSP00000497190.1:n.*1358C>G
ENST00000652304.1:c.*942C>G MANE Select	ENSP00000498622.1:n.*942C>G
ENST00000257979.4:c.*942C>G	ENSP00000257979.4:n.*942C>G
NM_012064.3:c.*942C>G	NP_036196.1:n.*942C>G
XM_011538354.1:c.*942C>G	XP_011536656.1:n.*942C>G
NM_012064.4:c.*942C>G MANE Select	NP_036196.1:n.*942C>G
XM_017019306.1:c.*942C>G	XP_016874795.1:n.*942C>G