Canonical Allele Identifier: CA2062458894

Gene: MVK MMAB

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109573481G= , CM000674.2:g.109573481G=	GRCh38
NC_000012.11:g.110011286G= , CM000674.1:g.110011286G=	GRCh37
NC_000012.10:g.108495669G=	NCBI36
NG_007096.1:g.5017C=
NG_007702.1:g.4787G= , LRG_156:g.4787G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000546277.6:c.-105G= (MVK)	ENSP00000438153.2:n.-105G=
ENST00000545712.7:c.-1C= (MMAB) MANE Select	ENSP00000445920.1:n.-1C=
ENST00000420167.6:c.-1C= (MMAB)	ENSP00000416136.2:n.-1C=
ENST00000503497.7:c.-1C= (MMAB)	ENSP00000474881.1:n.-1C=
ENST00000535044.1:n.141G= (MVK)
ENST00000536760.1:n.3C= (MMAB)
ENST00000537236.2:c.-1C= (MMAB)	ENSP00000483818.1:n.-1C=
ENST00000537496.5:c.-1C= (MMAB)	ENSP00000444793.1:n.-1C=
ENST00000539335.5:c.-96G= (MVK)	ENSP00000440379.1:n.-96G=
ENST00000540016.5:c.-1C= (MMAB)	ENSP00000474582.1:n.-1C=
ENST00000542390.5:n.27C= (MMAB)
ENST00000544051.5:c.-1C= (MMAB)	ENSP00000438079.1:n.-1C=
ENST00000545712.6:c.-1C= (MMAB)	ENSP00000445920.1:n.-1C=
ENST00000546277.5:c.-105G= (MVK)	ENSP00000438153.1:n.-105G=
NM_052845.3:c.-1C= (MMAB)	NP_443077.1:n.-1C=
NR_038118.1:n.73C= (MMAB)
XM_011538372.1:c.-105G= (MVK)	XP_011536674.1:n.-105G=
XM_024448961.1:c.-1C= (MMAB)	XP_024304729.1:n.-1C=
XM_024448982.1:c.-105G= (MVK)	XP_024304750.1:n.-105G=
NM_052845.4:c.-1C= (MMAB) MANE Select	NP_443077.1:n.-1C=
NR_038118.2:n.24C= (MMAB)