Canonical Allele Identifier: CA608509530

Gene: SLC15A4

Linked Data

• dbSNP Id: rs1251909034
• gnomAD v2: 12-129299631-G-A
• gnomAD v4: 12-128815086-G-A
• MyVariant Identifiers: chr12:g.129299631G>A (hg19) ; chr12:g.128815086G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815086G>A , CM000674.2:g.128815086G>A	GRCh38
NC_000012.11:g.129299631G>A , CM000674.1:g.129299631G>A	GRCh37
NC_000012.10:g.127865584G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.547-16C>T MANE Select	ENSP00000266771.5:n.547-16C>T
ENST00000266771.9:c.547-16C>T	ENSP00000266771.5:n.547-16C>T
ENST00000366292.6:n.843C>T
ENST00000376740.8:c.126-16C>T
ENST00000376744.8:c.383-16C>T
ENST00000535272.1:n.341-16C>T
ENST00000539703.1:n.197-16C>T
NM_145648.3:c.547-16C>T	NP_663623.1:n.547-16C>T
XM_011537895.1:c.697-16C>T	XP_011536197.1:n.697-16C>T
XR_429081.2:n.570-16C>T
XR_944494.1:n.720-16C>T
XR_944495.1:n.720-16C>T
XR_944496.1:n.720-16C>T
XR_944497.1:n.720-16C>T
XM_017018791.1:c.697-16C>T	XP_016874280.1:n.697-16C>T
XM_017018792.1:c.697-16C>T	XP_016874281.1:n.697-16C>T
XM_017018793.1:c.547-16C>T	XP_016874282.1:n.547-16C>T
XR_002957287.1:n.570-16C>T
XR_944496.2:n.720-16C>T
NM_145648.4:c.547-16C>T MANE Select	NP_663623.1:n.547-16C>T