Canonical Allele Identifier: CA6191417

Gene: MAP6

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75667629A>C , CM000673.2:g.75667629A>C	GRCh38
NC_000011.9:g.75378674A>C , CM000673.1:g.75378674A>C	GRCh37
NC_000011.8:g.75056322A>C	NCBI36
NG_052841.1:g.8480T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304771.8:c.741T>G MANE Select	ENSP00000307093.3:p.Ile247Met
ENST00000304771.7:c.741T>G	ENSP00000307093.3:p.Ile247Met
ENST00000434603.2:c.741T>G	ENSP00000415108.2:p.Ile247Met
ENST00000526740.3:c.-83+901T>G	ENSP00000434278.1:n.-83+901T>G
NM_033063.1:c.741T>G	NP_149052.1:p.Ile247Met
NM_207577.1:c.741T>G	NP_997460.1:p.Ile247Met
XM_006718556.2:c.741T>G	XP_006718619.1:p.Ile247Met
XM_011545039.1:c.741T>G	XP_011543341.1:p.Ile247Met
XR_949931.1:n.1102T>G
XR_949932.1:n.1102T>G
XR_949933.1:n.1102T>G
XM_006718556.4:c.741T>G	XP_006718619.1:p.Ile247Met
XM_011545039.3:c.741T>G	XP_011543341.1:p.Ile247Met
XM_017017755.2:c.741T>G	XP_016873244.1:p.Ile247Met
XR_949931.3:n.1096T>G
XR_949932.3:n.1096T>G
XR_949933.3:n.1096T>G
NM_033063.2:c.741T>G MANE Select	NP_149052.1:p.Ile247Met