Canonical Allele Identifier: CA2220108804
Gene: GPT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.46922434C= , CM000678.2:g.46922434C= GRCh38
NC_000016.9:g.46956346C= , CM000678.1:g.46956346C= GRCh37
NC_000016.8:g.45513847C= NCBI36
NG_042110.1:g.43055C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000340124.9:c.1212+18C= MANE Select ENSP00000345282.4:n.1212+18C=
ENST00000340124.8:c.1212+18C= ENSP00000345282.4:n.1212+18C=
ENST00000440783.2:c.912+18C= ENSP00000413804.2:n.912+18C=
ENST00000562801.5:n.1722+18C=
NM_001142466.1:c.912+18C= NP_001135938.1:n.912+18C=
NM_001142466.2:c.912+18C= NP_001135938.1:n.912+18C=
NM_133443.2:c.1212+18C= NP_597700.1:n.1212+18C=
NM_133443.3:c.1212+18C= NP_597700.1:n.1212+18C=
XM_017023790.1:c.780+18C= XP_016879279.1:n.780+18C=
NM_133443.4:c.1212+18C= MANE Select NP_597700.1:n.1212+18C=
NM_001142466.3:c.912+18C= NP_001135938.1:n.912+18C=