Canonical Allele Identifier: CA400362783

Gene: MTMR4

Linked Data

• MyVariant Identifiers: chr17:g.56584146C>A (hg19) ; chr17:g.58506785C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58506785C>A , CM000679.2:g.58506785C>A	GRCh38
NC_000017.10:g.56584146C>A , CM000679.1:g.56584146C>A	GRCh37
NC_000017.9:g.53939145C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682306.1:c.991G>T MANE Select	ENSP00000507664.1:p.Ala331Ser
ENST00000323456.9:c.949G>T	ENSP00000325285.5:p.Ala317Ser
ENST00000579925.5:c.949G>T	ENSP00000464067.1:p.Ala317Ser
NM_004687.4:c.949G>T	NP_004678.3:p.Ala317Ser
XM_005257784.2:c.991G>T	XP_005257841.1:p.Ala331Ser
XM_005257785.3:c.961G>T	XP_005257842.1:p.Ala321Ser
XM_005257786.3:c.949G>T	XP_005257843.1:p.Ala317Ser
XM_006722168.2:c.949G>T	XP_006722231.1:p.Ala317Ser
XM_011525460.1:c.961G>T	XP_011523762.1:p.Ala321Ser
XM_005257785.5:c.961G>T	XP_005257842.1:p.Ala321Ser
XM_005257786.5:c.949G>T	XP_005257843.1:p.Ala317Ser
XM_006722168.4:c.949G>T	XP_006722231.1:p.Ala317Ser
XM_011525460.3:c.961G>T	XP_011523762.1:p.Ala321Ser
NM_004687.5:c.949G>T	NP_004678.3:p.Ala317Ser
NM_001378066.1:c.961G>T	NP_001364995.1:p.Ala321Ser
NM_001378067.1:c.991G>T MANE Select	NP_001364996.1:p.Ala331Ser