Canonical Allele Identifier: CA386641680

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109573479A>T , CM000674.2:g.109573479A>T GRCh38
NC_000012.11:g.110011284A>T , CM000674.1:g.110011284A>T GRCh37
NC_000012.10:g.108495667A>T NCBI36
NG_007096.1:g.5019T>A
NG_007702.1:g.4785A>T , LRG_156:g.4785A>T

Transcript Alleles

HGVS Amino-acid Change
NM_052845.4:c.2T>A (MMAB) MANE Select NP_443077.1:p.Met1Lys
ENST00000545712.7:c.2T>A (MMAB) MANE Select ENSP00000445920.1:p.Met1Lys
NM_052845.3:c.2T>A (MMAB) NP_443077.1:p.Met1Lys
NR_038118.1:n.75T>A (MMAB)
NR_038118.2:n.26T>A (MMAB)
ENST00000420167.6:c.2T>A (MMAB) ENSP00000416136.2:p.Met1Lys
ENST00000503497.7:c.2T>A (MMAB) ENSP00000474881.1:p.Met1Lys
ENST00000535044.1:n.139A>T (MVK)
ENST00000536760.1:n.5T>A (MMAB)
ENST00000537236.2:c.2T>A (MMAB) ENSP00000483818.1:p.Met1Lys
ENST00000537496.5:c.2T>A (MMAB) ENSP00000444793.1:p.Met1Lys
ENST00000539335.5:c.-98A>T (MVK) ENSP00000440379.1:n.-98A>T
ENST00000540016.5:c.2T>A (MMAB) ENSP00000474582.1:p.Met1Lys
ENST00000541763.6:c.2T>A (MMAB) ENSP00000474981.1:p.Met1Lys
ENST00000542390.5:n.29T>A (MMAB)
ENST00000544051.5:c.2T>A (MMAB) ENSP00000438079.1:p.Met1Lys
ENST00000545712.6:c.2T>A (MMAB) ENSP00000445920.1:p.Met1Lys
ENST00000546277.5:c.-107A>T (MVK) ENSP00000438153.1:n.-107A>T
ENST00000546277.6:c.-107A>T (MVK) ENSP00000438153.2:n.-107A>T
XM_011538372.1:c.-107A>T (MVK) XP_011536674.1:n.-107A>T
XM_024448961.1:c.2T>A (MMAB) XP_024304729.1:p.Met1Lys
XM_024448982.1:c.-107A>T (MVK) XP_024304750.1:n.-107A>T