Canonical Allele Identifier: CA6190929

Gene: SERPINH1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75569024C>T , CM000673.2:g.75569024C>T	GRCh38
NC_000011.9:g.75280069C>T , CM000673.1:g.75280069C>T	GRCh37
NC_000011.8:g.74957717C>T	NCBI36
NG_012052.1:g.11900C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001235.5:c.807C>T MANE Select	NP_001226.2:p.Ile269=
ENST00000358171.8:c.807C>T MANE Select	ENSP00000350894.4:p.Ile269=
NM_001207014.1:c.807C>T	NP_001193943.1:p.Ile269=
NM_001207014.2:c.807C>T	NP_001193943.1:p.Ile269=
NM_001207014.3:c.807C>T	NP_001193943.1:p.Ile269=
NM_001235.3:c.807C>T	NP_001226.2:p.Ile269=
ENST00000358171.7:c.807C>T	ENSP00000350894.3:p.Ile269=
ENST00000524558.5:c.807C>T	ENSP00000434412.1:p.Ile269=
ENST00000525876.1:c.156C>T	ENSP00000433532.1:p.Ile52=
ENST00000530284.5:c.807C>T	ENSP00000436305.1:p.Ile269=
ENST00000532356.5:c.807C>T	ENSP00000436040.1:p.Ile269=
ENST00000533449.6:c.807C>T	ENSP00000431827.2:p.Ile269=
ENST00000533603.5:c.807C>T	ENSP00000434657.1:p.Ile269=
ENST00000649490.1:c.807C>T	ENSP00000497544.1:p.Ile269=
XM_006718729.1:c.807C>T	XP_006718792.1:p.Ile269=
XM_011545326.1:c.807C>T	XP_011543628.1:p.Ile269=
XM_011545327.1:c.807C>T	XP_011543629.1:p.Ile269=
XM_024448756.1:c.807C>T	XP_024304524.1:p.Ile269=