Canonical Allele Identifier: CA2621852455

Gene: SLC15A4

Linked Data

• gnomAD v4: 12-128815140-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815140C>A , CM000674.2:g.128815140C>A	GRCh38
NC_000012.11:g.129299685C>A , CM000674.1:g.129299685C>A	GRCh37
NC_000012.10:g.127865638C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.547-70G>T MANE Select	ENSP00000266771.5:n.547-70G>T
ENST00000266771.9:c.547-70G>T	ENSP00000266771.5:n.547-70G>T
ENST00000366292.6:n.789G>T
ENST00000376740.8:c.126-70G>T
ENST00000376744.8:c.383-70G>T
ENST00000535272.1:n.341-70G>T
ENST00000539703.1:n.197-70G>T
NM_145648.3:c.547-70G>T	NP_663623.1:n.547-70G>T
XM_011537895.1:c.697-70G>T	XP_011536197.1:n.697-70G>T
XR_429081.2:n.570-70G>T
XR_944494.1:n.720-70G>T
XR_944495.1:n.720-70G>T
XR_944496.1:n.720-70G>T
XR_944497.1:n.720-70G>T
XM_017018791.1:c.697-70G>T	XP_016874280.1:n.697-70G>T
XM_017018792.1:c.697-70G>T	XP_016874281.1:n.697-70G>T
XM_017018793.1:c.547-70G>T	XP_016874282.1:n.547-70G>T
XR_002957287.1:n.570-70G>T
XR_944496.2:n.720-70G>T
NM_145648.4:c.547-70G>T MANE Select	NP_663623.1:n.547-70G>T