Canonical Allele Identifier: CA2790190901

Gene: TH

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.2171657del , CM000673.2:g.2171657del	GRCh38
NC_000011.9:g.2192887del , CM000673.1:g.2192887del	GRCh37
NC_000011.8:g.2149463del	NCBI36
NG_008128.1:g.5150del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352909.8:c.90+41del MANE Select	ENSP00000325951.4:n.90+41del
ENST00000324155.8:c.90+41del	ENSP00000325831.3:n.90+41del
ENST00000333684.9:c.90+41del	ENSP00000328814.6:n.90+41del
ENST00000352909.7:c.90+41del	ENSP00000325951.3:n.90+41del
ENST00000381168.7:c.102+29del	ENSP00000370560.3:n.102+29del
ENST00000381175.5:c.90+41del	ENSP00000370567.1:n.90+41del
ENST00000381178.5:c.102+29del	ENSP00000370571.1:n.102+29del
NM_000360.3:c.90+41del	NP_000351.2:n.90+41del
NM_199292.2:c.102+29del	NP_954986.2:n.102+29del
NM_199293.2:c.90+41del	NP_954987.2:n.90+41del
XM_011520335.1:c.102+29del	XP_011518637.1:n.102+29del
XM_011520335.2:c.102+29del	XP_011518637.1:n.102+29del
NM_000360.4:c.90+41del MANE Select	NP_000351.2:n.90+41del
NM_199292.3:c.102+29del	NP_954986.2:n.102+29del
NM_199293.3:c.90+41del	NP_954987.2:n.90+41del