Canonical Allele Identifier: CA2062459001

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109573553T= , CM000674.2:g.109573553T= GRCh38
NC_000012.11:g.110011358T= , CM000674.1:g.110011358T= GRCh37
NC_000012.10:g.108495741T= NCBI36
NG_007096.1:g.4945A=
NG_007702.1:g.4859T= , LRG_156:g.4859T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000546277.6:c.-33T= (MVK) ENSP00000438153.2:n.-33T=
ENST00000535044.1:n.213T= (MVK)
ENST00000537236.2:c.-73A= (MMAB) ENSP00000483818.1:n.-73A=
ENST00000539335.5:c.-24T= (MVK) ENSP00000440379.1:n.-24T=
ENST00000545712.6:c.-73A= (MMAB) ENSP00000445920.1:n.-73A=
ENST00000546277.5:c.-33T= (MVK) ENSP00000438153.1:n.-33T=
NM_052845.3:c.-73A= (MMAB) NP_443077.1:n.-73A=
NR_038118.1:n.1A= (MMAB)
XM_011538372.1:c.-33T= (MVK) XP_011536674.1:n.-33T=
XM_017019313.2:c.-33T= (MVK) XP_016874802.1:n.-33T=
XM_024448961.1:c.-73A= (MMAB) XP_024304729.1:n.-73A=
XM_024448982.1:c.-33T= (MVK) XP_024304750.1:n.-33T=