Canonical Allele Identifier: CA373915568

Gene: SLC28A3

Linked Data

• MyVariant Identifiers: chr9:g.86905122C>G (hg19) ; chr9:g.84290207C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.84290207C>G , CM000671.2:g.84290207C>G	GRCh38
NC_000009.11:g.86905122C>G , CM000671.1:g.86905122C>G	GRCh37
NC_000009.10:g.86094942C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000376238.5:c.1096G>C MANE Select	ENSP00000365413.4:p.Ala366Pro
ENST00000376238.4:c.1096G>C	ENSP00000365413.4:p.Ala366Pro
NM_001199633.1:c.1096G>C	NP_001186562.1:p.Ala366Pro
NM_022127.2:c.1096G>C	NP_071410.1:p.Ala366Pro
NR_037638.2:n.1418G>C
XM_011518905.1:c.1180G>C	XP_011517207.1:p.Ala394Pro
XM_011518906.1:c.1180G>C	XP_011517208.1:p.Ala394Pro
XM_011518907.1:c.847G>C	XP_011517209.1:p.Ala283Pro
XM_011518908.1:c.457G>C	XP_011517210.1:p.Ala153Pro
XM_011518910.1:c.*113G>C	XP_011517212.1:n.*113G>C
XR_929832.1:n.1307G>C
XM_011518905.2:c.1180G>C	XP_011517207.1:p.Ala394Pro
XM_011518906.2:c.1180G>C	XP_011517208.1:p.Ala394Pro
XM_011518907.2:c.847G>C	XP_011517209.1:p.Ala283Pro
XM_011518908.2:c.457G>C	XP_011517210.1:p.Ala153Pro
XM_011518910.2:c.*113G>C	XP_011517212.1:n.*113G>C
XR_929832.2:n.1312G>C
NM_001199633.2:c.1096G>C MANE Select	NP_001186562.1:p.Ala366Pro
NM_022127.3:c.1096G>C	NP_071410.1:p.Ala366Pro
NR_037638.3:n.1397G>C