Canonical Allele Identifier: CA2062459065

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109573582T= , CM000674.2:g.109573582T= GRCh38
NC_000012.11:g.110011387T= , CM000674.1:g.110011387T= GRCh37
NC_000012.10:g.108495770T= NCBI36
NG_007096.1:g.4916A=
NG_007702.1:g.4888T= , LRG_156:g.4888T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000546277.6:c.-15+11T= (MVK) ENSP00000438153.2:n.-15+11T=
ENST00000535044.1:n.231+11T= (MVK)
ENST00000539335.5:c.-6+11T= (MVK) ENSP00000440379.1:n.-6+11T=
ENST00000545712.6:c.-102A= (MMAB) ENSP00000445920.1:n.-102A=
ENST00000546277.5:c.-15+11T= (MVK) ENSP00000438153.1:n.-15+11T=
XM_011538372.1:c.-15+11T= (MVK) XP_011536674.1:n.-15+11T=
XM_017019313.2:c.-15+11T= (MVK) XP_016874802.1:n.-15+11T=
XM_024448982.1:c.-15+11T= (MVK) XP_024304750.1:n.-15+11T=