Canonical Allele Identifier: CA358519381

Gene: MAP9

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.155347848G>C , CM000666.2:g.155347848G>C	GRCh38
NC_000004.11:g.156269000G>C , CM000666.1:g.156269000G>C	GRCh37
NC_000004.10:g.156488450G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001039580.2:c.1879C>G MANE Select	NP_001034669.1:p.Leu627Val
ENST00000311277.9:c.1879C>G MANE Select	ENSP00000310593.4:p.Leu627Val
NM_001039580.1:c.1879C>G	NP_001034669.1:p.Leu627Val
ENST00000311277.8:c.1879C>G	ENSP00000310593.4:p.Leu627Val
ENST00000515654.5:c.1807C>G	ENSP00000427402.1:p.Leu603Val
ENST00000650955.1:c.1879C>G	ENSP00000498412.1:p.Leu627Val
XM_006714306.2:c.1876C>G	XP_006714369.1:p.Leu626Val
XM_006714306.4:c.1876C>G	XP_006714369.1:p.Leu626Val
XM_011532253.1:c.1879C>G	XP_011530555.1:p.Leu627Val
XM_011532254.1:c.1879C>G	XP_011530556.1:p.Leu627Val
XM_011532254.2:c.1879C>G	XP_011530556.1:p.Leu627Val
XM_011532255.1:c.1663C>G	XP_011530557.1:p.Leu555Val
XM_011532255.3:c.1663C>G	XP_011530557.1:p.Leu555Val
XM_017008616.1:c.1876C>G	XP_016864105.1:p.Leu626Val
XM_017008617.1:c.1876C>G	XP_016864106.1:p.Leu626Val