Canonical Allele Identifier: CA408132037
Gene: HSPA12B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3740838G>T , CM000682.2:g.3740838G>T GRCh38
NC_000020.10:g.3721485G>T , CM000682.1:g.3721485G>T GRCh37
NC_000020.9:g.3669485G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000254963.7:c.67G>T MANE Select ENSP00000254963.2:p.Val23Leu
ENST00000254963.6:c.67G>T ENSP00000254963.2:p.Val23Leu
ENST00000399701.1:c.-117-1446G>T ENSP00000382608.1:n.-117-1446G>T
NM_001197327.1:c.67G>T NP_001184256.1:p.Val23Leu
NM_052970.4:c.67G>T NP_443202.3:p.Val23Leu
XM_005260656.2:c.-117-1446G>T XP_005260713.1:n.-117-1446G>T
XM_011529149.1:c.139G>T XP_011527451.1:p.Val47Leu
XM_011529150.1:c.139G>T XP_011527452.1:p.Val47Leu
XM_011529152.1:c.139G>T XP_011527454.1:p.Val47Leu
NM_001318322.1:c.-117-1446G>T NP_001305251.1:n.-117-1446G>T
XM_017027632.2:c.67G>T XP_016883121.1:p.Val23Leu
XM_017027633.1:c.67G>T XP_016883122.1:p.Val23Leu
XM_017027634.1:c.67G>T XP_016883123.1:p.Val23Leu
XM_017027635.1:c.67G>T XP_016883124.1:p.Val23Leu
NM_052970.5:c.67G>T MANE Select NP_443202.3:p.Val23Leu
NM_001197327.2:c.67G>T NP_001184256.1:p.Val23Leu
NM_001318322.2:c.-117-1446G>T NP_001305251.1:n.-117-1446G>T