Canonical Allele Identifier: CA2566847570

Gene: MIP

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450059A>G , CM000674.2:g.56450059A>G	GRCh38
NC_000012.11:g.56843843A>G , CM000674.1:g.56843843A>G	GRCh37
NC_000012.10:g.55130110A>G	NCBI36
NG_021397.1:g.9593T>C
NG_021397.2:g.24108T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1637T>C	ENSP00000497190.1:n.*1637T>C
ENST00000652304.1:c.*1221T>C MANE Select	ENSP00000498622.1:n.*1221T>C
ENST00000257979.4:c.*1221T>C	ENSP00000257979.4:n.*1221T>C
NM_012064.3:c.*1221T>C	NP_036196.1:n.*1221T>C
XM_011538354.1:c.*1221T>C	XP_011536656.1:n.*1221T>C
NM_012064.4:c.*1221T>C MANE Select	NP_036196.1:n.*1221T>C
XM_017019306.1:c.*1221T>C	XP_016874795.1:n.*1221T>C