Canonical Allele Identifier: CA2143948136

Gene: PIGH GPHN

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.67600203T= , CM000676.2:g.67600203T=	GRCh38
NC_000014.8:g.68066920T= , CM000676.1:g.68066920T=	GRCh37
NC_000014.7:g.67136673T=	NCBI36
NG_050632.2:g.5100A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004569.5:c.1A= (PIGH) MANE Select	NP_004560.1:p.Met1=
ENST00000216452.9:c.1A= (PIGH) MANE Select	ENSP00000216452.4:p.Met1=
NM_001363694.1:c.1A= (PIGH)	NP_001350623.1:p.Met1=
NM_004569.3:c.1A= (PIGH)	NP_004560.1:p.Met1=
NM_004569.4:c.1A= (PIGH)	NP_004560.1:p.Met1=
ENST00000216452.8:c.1A= (PIGH)	ENSP00000216452.4:p.Met1=
ENST00000558001.1:c.1A= (PIGH)	ENSP00000454061.1:p.Met1=
ENST00000558198.5:c.1A= (PIGH)	ENSP00000452924.1:p.Met1=
ENST00000559097.1:n.84A= (PIGH)
ENST00000559415.1:c.1A= (PIGH)	ENSP00000452996.1:p.Met1=
ENST00000559581.5:c.1A= (PIGH)	ENSP00000453733.1:p.Met1=
ENST00000560722.5:c.1A= (PIGH)	ENSP00000453394.1:p.Met1=
ENST00000561303.5:c.1A= (PIGH)	ENSP00000452974.1:p.Met1=
XM_006720172.2:c.-7A= (PIGH)	XP_006720235.1:n.-7A=
XM_011536838.1:c.1A= (PIGH)	XP_011535140.1:p.Met1=
XM_011536838.3:c.1A= (PIGH)	XP_011535140.1:p.Met1=
XM_017020925.2:c.1313-134992T= (GPHN)	XP_016876414.1:n.1313-134992T=
XM_017021371.2:c.1A= (PIGH)	XP_016876860.1:p.Met1=
XR_943477.1:n.98A= (PIGH)