Canonical Allele Identifier: CA162520594

Gene: STEAP4

Linked Data

• dbSNP Id: rs1018985780
• gnomAD v3: 7-88297941-G-A
• gnomAD v4: 7-88297941-G-A
• MyVariant Identifiers: chr7:g.87927256G>A (hg19) ; chr7:g.88297941G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.88297941G>A , CM000669.2:g.88297941G>A	GRCh38
NC_000007.13:g.87927256G>A , CM000669.1:g.87927256G>A	GRCh37
NC_000007.12:g.87765192G>A	NCBI36
NG_028313.1:g.13973C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380079.9:c.-3+8851C>T MANE Select	ENSP00000369419.4:n.-3+8851C>T
ENST00000301959.9:c.-3+8851C>T	ENSP00000305545.5:n.-3+8851C>T
ENST00000380079.8:c.-3+8851C>T	ENSP00000369419.4:n.-3+8851C>T
ENST00000414498.1:c.-101-6927C>T	ENSP00000394399.1:n.-101-6927C>T
NM_001205315.1:c.-101-6927C>T	NP_001192244.1:n.-101-6927C>T
NM_001205316.1:c.-3+8851C>T	NP_001192245.1:n.-3+8851C>T
NM_024636.3:c.-3+8851C>T	NP_078912.2:n.-3+8851C>T
NM_001205315.2:c.-101-6927C>T	NP_001192244.1:n.-101-6927C>T
NM_001205316.2:c.-3+8851C>T	NP_001192245.1:n.-3+8851C>T
NM_024636.4:c.-3+8851C>T MANE Select	NP_078912.2:n.-3+8851C>T