Canonical Allele Identifier: CA539321374

Gene: MAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.209506195dup , CM000664.2:g.209506195dup	GRCh38
NC_000002.11:g.210370919dup , CM000664.1:g.210370919dup	GRCh37
NC_000002.10:g.210079164dup	NCBI36
NG_052836.1:g.87149dup

Transcript Alleles

HGVS	Amino-acid Change
NM_001375505.1:c.-221-1397dup MANE Select	NP_001362434.1:n.-221-1397dup
ENST00000682079.1:c.-221-1397dup MANE Select	ENSP00000507035.1:n.-221-1397dup
NM_001039538.1:c.-221-1397dup	NP_001034627.1:n.-221-1397dup
NM_001039538.2:c.-221-1397dup	NP_001034627.1:n.-221-1397dup
NM_001363910.1:c.-221-1397dup	NP_001350839.1:n.-221-1397dup
NM_001363910.2:c.-221-1397dup	NP_001350839.1:n.-221-1397dup
NM_001375474.1:c.-221-1397dup	NP_001362403.1:n.-221-1397dup
NM_001375493.1:c.-221-1397dup	NP_001362422.1:n.-221-1397dup
NM_001375494.1:c.-171-73841dup	NP_001362423.1:n.-171-73841dup
NM_001375495.1:c.-221-1397dup	NP_001362424.1:n.-221-1397dup
NM_001375496.1:c.-221-1397dup	NP_001362425.1:n.-221-1397dup
NM_001375497.1:c.-221-1397dup	NP_001362426.1:n.-221-1397dup
NM_001375498.1:c.-221-1397dup	NP_001362427.1:n.-221-1397dup
NM_001375499.1:c.-171-73841dup	NP_001362428.1:n.-171-73841dup
NM_001375500.1:c.-221-1397dup	NP_001362429.1:n.-221-1397dup
NM_001375501.1:c.-221-1397dup	NP_001362430.1:n.-221-1397dup
NM_001375502.1:c.-171-73841dup	NP_001362431.1:n.-171-73841dup
NM_001375503.1:c.-221-1397dup	NP_001362432.1:n.-221-1397dup
NM_001375504.1:c.-221-1397dup	NP_001362433.1:n.-221-1397dup
NM_001375506.1:c.-221-1397dup	NP_001362435.1:n.-221-1397dup
NM_001375507.1:c.-221-1397dup	NP_001362436.1:n.-221-1397dup
NM_001375508.1:c.-221-1397dup	NP_001362437.1:n.-221-1397dup
NM_001375583.1:c.-221-1397dup	NP_001362512.1:n.-221-1397dup
ENST00000199940.10:c.-221-1397dup	ENSP00000199940.6:n.-221-1397dup
ENST00000704357.1:c.-221-1397dup	ENSP00000515868.1:n.-221-1397dup
XM_011511195.2:c.-221-1397dup	XP_011509497.1:n.-221-1397dup
XM_017004116.2:c.-221-1397dup	XP_016859605.1:n.-221-1397dup
XM_017004128.2:c.-221-1397dup	XP_016859617.1:n.-221-1397dup
XM_017004129.2:c.-221-1397dup	XP_016859618.1:n.-221-1397dup
XM_024452891.1:c.-221-1397dup	XP_024308659.1:n.-221-1397dup
XM_024452894.1:c.-221-1397dup	XP_024308662.1:n.-221-1397dup
XM_024452895.1:c.-221-1397dup	XP_024308663.1:n.-221-1397dup
XM_024452896.1:c.-221-1397dup	XP_024308664.1:n.-221-1397dup
XM_024452897.1:c.-221-1397dup	XP_024308665.1:n.-221-1397dup
XM_024452899.1:c.-221-1397dup	XP_024308667.1:n.-221-1397dup
XM_024452900.1:c.-221-1397dup	XP_024308668.1:n.-221-1397dup
XM_024452901.1:c.-221-1397dup	XP_024308669.1:n.-221-1397dup
XM_024452902.1:c.-221-1397dup	XP_024308670.1:n.-221-1397dup
XM_024452905.1:c.-221-1397dup	XP_024308673.1:n.-221-1397dup
XM_024452906.1:c.-221-1397dup	XP_024308674.1:n.-221-1397dup
XM_024452907.1:c.-221-1397dup	XP_024308675.1:n.-221-1397dup
XM_024452910.1:c.-221-1397dup	XP_024308678.1:n.-221-1397dup
XM_024452911.1:c.-221-1397dup	XP_024308679.1:n.-221-1397dup