Canonical Allele Identifier: CA120032108

Gene: MAP1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.72194500G>A , CM000667.2:g.72194500G>A	GRCh38
NC_000005.9:g.71490327G>A , CM000667.1:g.71490327G>A	GRCh37
NC_000005.8:g.71526083G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296755.12:c.1145G>A MANE Select	ENSP00000296755.7:p.Cys382Tyr
ENST00000296755.11:c.1145G>A	ENSP00000296755.7:p.Cys382Tyr
ENST00000504492.1:c.767G>A	ENSP00000423416.1:p.Cys256Tyr
ENST00000511641.2:c.1196G>A	ENSP00000423444.2:p.Cys399Tyr
ENST00000513526.6:c.*865G>A	ENSP00000427194.2:n.*865G>A
NM_005909.3:c.1145G>A	NP_005900.2:p.Cys382Tyr
XM_005248507.2:c.767G>A	XP_005248564.1:p.Cys256Tyr
NM_001324255.1:c.767G>A	NP_001311184.1:p.Cys256Tyr
NM_005909.4:c.1145G>A	NP_005900.2:p.Cys382Tyr
NM_005909.5:c.1145G>A MANE Select	NP_005900.2:p.Cys382Tyr
NM_001324255.2:c.767G>A	NP_001311184.1:p.Cys256Tyr