Canonical Allele Identifier: CA2062458976

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109573541T= , CM000674.2:g.109573541T= GRCh38
NC_000012.11:g.110011346T= , CM000674.1:g.110011346T= GRCh37
NC_000012.10:g.108495729T= NCBI36
NG_007096.1:g.4957A=
NG_007702.1:g.4847T= , LRG_156:g.4847T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000546277.6:c.-45T= (MVK) ENSP00000438153.2:n.-45T=
ENST00000535044.1:n.201T= (MVK)
ENST00000537236.2:c.-61A= (MMAB) ENSP00000483818.1:n.-61A=
ENST00000539335.5:c.-36T= (MVK) ENSP00000440379.1:n.-36T=
ENST00000545712.6:c.-61A= (MMAB) ENSP00000445920.1:n.-61A=
ENST00000546277.5:c.-45T= (MVK) ENSP00000438153.1:n.-45T=
NM_052845.3:c.-61A= (MMAB) NP_443077.1:n.-61A=
NR_038118.1:n.13A= (MMAB)
XM_011538372.1:c.-45T= (MVK) XP_011536674.1:n.-45T=
XM_017019313.2:c.-45T= (MVK) XP_016874802.1:n.-45T=
XM_024448961.1:c.-61A= (MMAB) XP_024304729.1:n.-61A=
XM_024448982.1:c.-45T= (MVK) XP_024304750.1:n.-45T=