Canonical Allele Identifier: CA377782396

Gene: MINPP1

Linked Data

• MyVariant Identifiers: chr10:g.89268097G>C (hg19) ; chr10:g.87508340G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87508340G>C , CM000672.2:g.87508340G>C	GRCh38
NC_000010.10:g.89268097G>C , CM000672.1:g.89268097G>C	GRCh37
NC_000010.9:g.89258077G>C	NCBI36
NG_013023.1:g.8875G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371996.9:c.642G>C MANE Select	ENSP00000361064.4:p.Met214Ile
ENST00000371994.8:c.642G>C	ENSP00000361062.4:p.Met214Ile
ENST00000371996.8:c.642G>C	ENSP00000361064.4:p.Met214Ile
ENST00000536010.1:c.39G>C	ENSP00000437823.1:p.Met13Ile
NM_001178117.1:c.642G>C	NP_001171588.1:p.Met214Ile
NM_001178118.1:c.39G>C	NP_001171589.1:p.Met13Ile
NM_004897.4:c.642G>C	NP_004888.2:p.Met214Ile
XM_006718078.2:c.642G>C	XP_006718141.1:p.Met214Ile
XM_011540379.1:c.39G>C	XP_011538681.1:p.Met13Ile
XR_945884.1:n.2766G>C
XM_006718078.3:c.642G>C	XP_006718141.1:p.Met214Ile
XM_011540379.3:c.39G>C	XP_011538681.1:p.Met13Ile
XM_017016965.2:c.642G>C	XP_016872454.1:p.Met214Ile
NM_004897.5:c.642G>C MANE Select	NP_004888.2:p.Met214Ile
NM_001178117.2:c.642G>C	NP_001171588.1:p.Met214Ile
NM_001178118.2:c.39G>C	NP_001171589.1:p.Met13Ile