Canonical Allele Identifier: CA468656447

Gene: THNSL1 ENKUR

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.25023619T>G , CM000672.2:g.25023619T>G	GRCh38
NC_000010.10:g.25312548T>G , CM000672.1:g.25312548T>G	GRCh37
NC_000010.9:g.25352554T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376356.5:c.396T>G (THNSL1) MANE Select	ENSP00000365534.4:p.Thr132=
ENST00000376356.4:c.396T>G (THNSL1)	ENSP00000365534.4:p.Thr132=
ENST00000524413.5:c.396T>G (THNSL1)	ENSP00000434887.1:p.Thr132=
ENST00000615958.4:c.38-27750A>C (ENKUR)	ENSP00000478989.1:n.38-27750A>C
NM_001270383.1:c.38-27750A>C (ENKUR)	NP_001257312.1:n.38-27750A>C
NM_024838.4:c.396T>G (THNSL1)	NP_079114.3:p.Thr132=
XM_005252597.1:c.396T>G (THNSL1)	XP_005252654.1:p.Thr132=
XM_005252597.3:c.396T>G (THNSL1)	XP_005252654.1:p.Thr132=
XM_017016665.1:c.396T>G (THNSL1)	XP_016872154.1:p.Thr132=
NM_024838.5:c.396T>G (THNSL1) MANE Select	NP_079114.3:p.Thr132=
NM_001270383.2:c.38-27750A>C (ENKUR)	NP_001257312.1:n.38-27750A>C