Canonical Allele Identifier: CA1723965618

Gene: STEAP4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.88298132T= , CM000669.2:g.88298132T=	GRCh38
NC_000007.13:g.87927447T= , CM000669.1:g.87927447T=	GRCh37
NC_000007.12:g.87765383T=	NCBI36
NG_028313.1:g.13782A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000380079.9:c.-3+8660A= MANE Select	ENSP00000369419.4:n.-3+8660A=
ENST00000301959.9:c.-3+8660A=	ENSP00000305545.5:n.-3+8660A=
ENST00000380079.8:c.-3+8660A=	ENSP00000369419.4:n.-3+8660A=
ENST00000414498.1:c.-101-7118A=	ENSP00000394399.1:n.-101-7118A=
NM_001205315.1:c.-101-7118A=	NP_001192244.1:n.-101-7118A=
NM_001205316.1:c.-3+8660A=	NP_001192245.1:n.-3+8660A=
NM_024636.3:c.-3+8660A=	NP_078912.2:n.-3+8660A=
NM_001205315.2:c.-101-7118A=	NP_001192244.1:n.-101-7118A=
NM_001205316.2:c.-3+8660A=	NP_001192245.1:n.-3+8660A=
NM_024636.4:c.-3+8660A= MANE Select	NP_078912.2:n.-3+8660A=