Canonical Allele Identifier: CA162520614

Gene: STEAP4

Linked Data

• dbSNP Id: rs1042456638
• gnomAD v3: 7-88298123-T-C
• gnomAD v4: 7-88298123-T-C
• MyVariant Identifiers: chr7:g.87927438T>C (hg19) ; chr7:g.88298123T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.88298123T>C , CM000669.2:g.88298123T>C	GRCh38
NC_000007.13:g.87927438T>C , CM000669.1:g.87927438T>C	GRCh37
NC_000007.12:g.87765374T>C	NCBI36
NG_028313.1:g.13791A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000380079.9:c.-3+8669A>G MANE Select	ENSP00000369419.4:n.-3+8669A>G
ENST00000301959.9:c.-3+8669A>G	ENSP00000305545.5:n.-3+8669A>G
ENST00000380079.8:c.-3+8669A>G	ENSP00000369419.4:n.-3+8669A>G
ENST00000414498.1:c.-101-7109A>G	ENSP00000394399.1:n.-101-7109A>G
NM_001205315.1:c.-101-7109A>G	NP_001192244.1:n.-101-7109A>G
NM_001205316.1:c.-3+8669A>G	NP_001192245.1:n.-3+8669A>G
NM_024636.3:c.-3+8669A>G	NP_078912.2:n.-3+8669A>G
NM_001205315.2:c.-101-7109A>G	NP_001192244.1:n.-101-7109A>G
NM_001205316.2:c.-3+8669A>G	NP_001192245.1:n.-3+8669A>G
NM_024636.4:c.-3+8669A>G MANE Select	NP_078912.2:n.-3+8669A>G