Canonical Allele Identifier: CA843477465

Gene: STEAP4

Linked Data

• dbSNP Id: rs1431904034
• MyVariant Identifiers: chr7:g.87927446A>G (hg19) ; chr7:g.88298131A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.88298131A>G , CM000669.2:g.88298131A>G	GRCh38
NC_000007.13:g.87927446A>G , CM000669.1:g.87927446A>G	GRCh37
NC_000007.12:g.87765382A>G	NCBI36
NG_028313.1:g.13783T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000380079.9:c.-3+8661T>C MANE Select	ENSP00000369419.4:n.-3+8661T>C
ENST00000301959.9:c.-3+8661T>C	ENSP00000305545.5:n.-3+8661T>C
ENST00000380079.8:c.-3+8661T>C	ENSP00000369419.4:n.-3+8661T>C
ENST00000414498.1:c.-101-7117T>C	ENSP00000394399.1:n.-101-7117T>C
NM_001205315.1:c.-101-7117T>C	NP_001192244.1:n.-101-7117T>C
NM_001205316.1:c.-3+8661T>C	NP_001192245.1:n.-3+8661T>C
NM_024636.3:c.-3+8661T>C	NP_078912.2:n.-3+8661T>C
NM_001205315.2:c.-101-7117T>C	NP_001192244.1:n.-101-7117T>C
NM_001205316.2:c.-3+8661T>C	NP_001192245.1:n.-3+8661T>C
NM_024636.4:c.-3+8661T>C MANE Select	NP_078912.2:n.-3+8661T>C