Canonical Allele Identifier: CA027686

Gene: NTHL1 TSC2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2047817C>A , CM000678.2:g.2047817C>A	GRCh38
NC_000016.9:g.2097818C>A , CM000678.1:g.2097818C>A	GRCh37
NC_000016.8:g.2037819C>A	NCBI36
NG_005895.1:g.3512C>A , LRG_487:g.3512C>A
NG_008412.1:g.5050G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002528.7:c.7G>T (NTHL1) MANE Select	NP_002519.2:p.Ala3Ser
ENST00000651570.2:c.7G>T (NTHL1) MANE Select	ENSP00000498421.1:p.Ala3Ser
NM_001318193.1:c.31G>T (NTHL1)	NP_001305122.1:p.Ala11Ser
NM_001318193.2:c.7G>T (NTHL1)	NP_001305122.2:p.Ala3Ser
NM_001318194.1:c.-172G>T (NTHL1)	NP_001305123.1:n.-172G>T
NM_001318194.2:c.-172G>T (NTHL1)	NP_001305123.1:n.-172G>T
NM_002528.5:c.31G>T (NTHL1)	NP_002519.1:p.Ala11Ser
NM_002528.6:c.31G>T (NTHL1)	NP_002519.1:p.Ala11Ser
ENST00000219066.5:c.31G>T (NTHL1)	ENSP00000219066.1:p.Ala11Ser
ENST00000219476.7:c.-278C>A (TSC2)	ENSP00000219476.3:n.-278C>A
ENST00000623977.1:n.31G>T (NTHL1)
XM_011522505.1:c.31G>T (NTHL1)	XP_011520807.1:p.Ala11Ser
XM_011522638.2:c.-5C>A (TSC2)	XP_011520940.2:n.-5C>A
XM_017023253.1:c.31G>T (NTHL1)	XP_016878742.1:p.Ala11Ser
XM_017023617.1:c.-5C>A (TSC2)	XP_016879106.1:n.-5C>A