Canonical Allele Identifier: CA170544
Gene: SALL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.21525643C>A , CM000676.2:g.21525643C>A GRCh38
NC_000014.8:g.21993777C>A , CM000676.1:g.21993777C>A GRCh37
NC_000014.7:g.21063617C>A NCBI36
NG_051069.1:g.16574G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001364564.1:c.79G>T MANE Select NP_001351493.1:p.Glu27Ter
ENST00000537235.2:c.79G>T MANE Select ENSP00000438493.2:p.Glu27Ter
NM_001291446.1:c.85G>T NP_001278375.1:p.Glu29Ter
NM_001291446.2:c.85G>T NP_001278375.1:p.Glu29Ter
NM_001291447.1:c.79G>T NP_001278376.1:p.Glu27Ter
NM_001291447.2:c.79G>T NP_001278376.1:p.Glu27Ter
NM_005407.2:c.85G>T NP_005398.2:p.Glu29Ter
NM_005407.3:c.85G>T NP_005398.2:p.Glu29Ter
NR_111966.1:n.380G>T
NR_111966.2:n.285G>T
NR_111967.1:n.360G>T
NR_111967.2:n.298G>T
ENST00000450879.2:c.79G>T ENSP00000396773.2:p.Glu27Ter
ENST00000537235.1:c.79G>T ENSP00000438493.1:p.Glu27Ter
ENST00000541965.1:c.-102G>T ENSP00000439654.1:n.-102G>T
ENST00000546363.5:c.66G>T
ENST00000611430.4:c.79G>T ENSP00000484460.1:p.Glu27Ter
ENST00000613414.4:c.85G>T ENSP00000483202.1:p.Glu29Ter
ENST00000614342.1:c.85G>T ENSP00000483562.1:p.Glu29Ter
XM_011537064.1:c.85G>T XP_011535366.1:p.Glu29Ter
XM_011537065.1:c.79G>T XP_011535367.1:p.Glu27Ter
XM_011537065.2:c.79G>T XP_011535367.1:p.Glu27Ter