Canonical Allele Identifier: CA1492770934

Gene: HSPA4L

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.127811775A= , CM000666.2:g.127811775A=	GRCh38
NC_000004.11:g.128732930A= , CM000666.1:g.128732930A=	GRCh37
NC_000004.10:g.128952380A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000296464.9:c.1578+139A= MANE Select	ENSP00000296464.3:n.1578+139A=
ENST00000296464.8:c.1578+139A=	ENSP00000296464.3:n.1578+139A=
ENST00000505726.1:c.1500+139A=	ENSP00000425645.1:n.1500+139A=
ENST00000508549.5:c.1455+139A=	ENSP00000427305.1:n.1455+139A=
ENST00000508776.5:c.1578+139A=	ENSP00000422482.1:n.1578+139A=
NM_014278.2:c.1578+139A=	NP_055093.2:n.1578+139A=
XM_011531744.1:c.1500+139A=	XP_011530046.1:n.1500+139A=
NM_001317381.1:c.1671+139A=	NP_001304310.1:n.1671+139A=
NM_001317382.1:c.1500+139A=	NP_001304311.1:n.1500+139A=
NM_001317383.1:c.1455+139A=	NP_001304312.1:n.1455+139A=
NM_014278.3:c.1578+139A=	NP_055093.2:n.1578+139A=
NM_014278.4:c.1578+139A= MANE Select	NP_055093.2:n.1578+139A=
NM_001317381.2:c.1671+139A=	NP_001304310.1:n.1671+139A=
NM_001317383.2:c.1455+139A=	NP_001304312.1:n.1455+139A=
NM_001317382.2:c.1500+139A=	NP_001304311.1:n.1500+139A=