Canonical Allele Identifier: CA2621852354

Gene: SLC15A4

Linked Data

• gnomAD v4: 12-128814668-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814668G>T , CM000674.2:g.128814668G>T	GRCh38
NC_000012.11:g.129299213G>T , CM000674.1:g.129299213G>T	GRCh37
NC_000012.10:g.127865166G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.842+107C>A MANE Select	ENSP00000266771.5:n.842+107C>A
ENST00000266771.9:c.842+107C>A	ENSP00000266771.5:n.842+107C>A
ENST00000366292.6:n.1154+107C>A
ENST00000376740.8:c.421+107C>A
ENST00000376744.8:c.678+107C>A
ENST00000539703.1:n.492+107C>A
ENST00000614634.1:c.-1+107C>A	ENSP00000483143.1:n.-1+107C>A
NM_145648.3:c.842+107C>A	NP_663623.1:n.842+107C>A
XM_011537895.1:c.992+107C>A	XP_011536197.1:n.992+107C>A
XR_429081.2:n.865+107C>A
XR_944494.1:n.1015+107C>A
XR_944495.1:n.1015+107C>A
XR_944496.1:n.1015+107C>A
XR_944497.1:n.1015+107C>A
XM_017018791.1:c.992+107C>A	XP_016874280.1:n.992+107C>A
XM_017018792.1:c.992+107C>A	XP_016874281.1:n.992+107C>A
XM_017018793.1:c.842+107C>A	XP_016874282.1:n.842+107C>A
XR_002957287.1:n.865+107C>A
XR_944496.2:n.1015+107C>A
NM_145648.4:c.842+107C>A MANE Select	NP_663623.1:n.842+107C>A