Canonical Allele Identifier: CA2315330276

Gene: MBP

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.77095185C>G , CM000680.2:g.77095185C>G	GRCh38
NC_000018.9:g.74807141C>G , CM000680.1:g.74807141C>G	GRCh37
NC_000018.8:g.72936129C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355994.7:c.51+10026G>C MANE Select	ENSP00000348273.2:n.51+10026G>C
ENST00000355994.6:c.51+10026G>C	ENSP00000348273.2:n.51+10026G>C
ENST00000397860.7:c.51+10026G>C	ENSP00000380958.3:n.51+10026G>C
ENST00000397863.5:c.51+10026G>C	ENSP00000380961.1:n.51+10026G>C
ENST00000487778.5:n.535+2066G>C
ENST00000490754.5:n.244+10026G>C
ENST00000497479.1:n.651+183G>C
ENST00000579129.5:c.51+10026G>C	ENSP00000463780.1:n.51+10026G>C
ENST00000580402.5:c.51+10026G>C	ENSP00000462223.1:n.51+10026G>C
ENST00000581878.5:c.51+10026G>C	ENSP00000462374.1:n.51+10026G>C
ENST00000583798.1:c.51+10026G>C	ENSP00000463164.1:n.51+10026G>C
NM_001025100.1:c.51+10026G>C	NP_001020271.1:n.51+10026G>C
NM_001025101.1:c.51+10026G>C	NP_001020272.1:n.51+10026G>C
XM_011526008.1:c.51+10026G>C	XP_011524310.1:n.51+10026G>C
XM_011526009.1:c.51+10026G>C	XP_011524311.1:n.51+10026G>C
XM_011526010.1:c.51+10026G>C	XP_011524312.1:n.51+10026G>C
XM_011526011.1:c.51+10026G>C	XP_011524313.1:n.51+10026G>C
XM_011526012.1:c.51+10026G>C	XP_011524314.1:n.51+10026G>C
XR_245460.2:n.310+10026G>C
XR_245461.2:n.310+10026G>C
XM_017025778.2:c.223+10026G>C	XP_016881267.1:n.223+10026G>C
XM_017025780.2:c.51+10026G>C	XP_016881269.1:n.51+10026G>C
XM_024451185.1:c.51+10026G>C	XP_024306953.1:n.51+10026G>C
XM_024451186.1:c.51+10026G>C	XP_024306954.1:n.51+10026G>C
XM_024451187.1:c.51+10026G>C	XP_024306955.1:n.51+10026G>C
NM_001025101.2:c.51+10026G>C MANE Select	NP_001020272.1:n.51+10026G>C
NM_001025100.2:c.51+10026G>C	NP_001020271.1:n.51+10026G>C