Canonical Allele Identifier: CA2362880624
Gene: TGM2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.38165145C= , CM000682.2:g.38165145C= GRCh38
NC_000020.10:g.36793547C= , CM000682.1:g.36793547C= GRCh37
NC_000020.9:g.36226961C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000361475.7:c.10+44G= MANE Select ENSP00000355330.2:n.10+44G=
ENST00000361475.6:c.10+44G= ENSP00000355330.2:n.10+44G=
ENST00000373403.7:c.10+44G= ENSP00000362502.3:n.10+44G=
ENST00000453095.1:c.10+44G= ENSP00000387642.1:n.10+44G=
ENST00000468262.5:n.94+44G=
ENST00000474777.1:n.71+44G=
NM_004613.2:c.10+44G= NP_004604.2:n.10+44G=
NM_198951.1:c.10+44G= NP_945189.1:n.10+44G=
XM_011529028.1:c.10+44G= XP_011527330.1:n.10+44G=
XM_011529029.1:c.10+44G= XP_011527331.1:n.10+44G=
NM_001323316.1:c.10+44G= NP_001310245.1:n.10+44G=
NM_001323317.1:c.10+44G= NP_001310246.1:n.10+44G=
NM_001323318.1:c.10+44G= NP_001310247.1:n.10+44G=
NM_004613.3:c.10+44G= NP_004604.2:n.10+44G=
NM_198951.2:c.10+44G= NP_945189.1:n.10+44G=
XR_001754586.1:n.34G=
NM_004613.4:c.10+44G= MANE Select NP_004604.2:n.10+44G=
NM_001323316.2:c.10+44G= NP_001310245.1:n.10+44G=
NM_001323317.2:c.10+44G= NP_001310246.1:n.10+44G=
NM_001323318.2:c.10+44G= NP_001310247.1:n.10+44G=
NM_198951.3:c.10+44G= NP_945189.1:n.10+44G=