Canonical Allele Identifier: CA697461873

Gene: STARD13

Linked Data

• dbSNP Id: rs1392026132
• MyVariant Identifiers: chr13:g.33798187A>G (hg19) ; chr13:g.33224050A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.33224050A>G , CM000675.2:g.33224050A>G	GRCh38
NC_000013.10:g.33798187A>G , CM000675.1:g.33798187A>G	GRCh37
NC_000013.9:g.32696187A>G	NCBI36
NG_029752.1:g.66715T>C
NG_029752.2:g.457786T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000567873.2:c.125-56428T>C	ENSP00000456233.2:n.125-56428T>C
ENST00000336934.10:c.170-56428T>C MANE Select	ENSP00000338785.4:n.170-56428T>C
ENST00000336934.9:c.170-56428T>C	ENSP00000338785.4:n.170-56428T>C
ENST00000487412.5:n.287-56428T>C
ENST00000498019.2:n.239-56428T>C
ENST00000567873.1:c.125-56428T>C	ENSP00000456233.1:n.125-56428T>C
NM_001243476.2:c.65-56428T>C	NP_001230405.1:n.65-56428T>C
NM_178006.3:c.170-56428T>C	NP_821074.1:n.170-56428T>C
XM_011535298.1:c.203-56428T>C	XP_011533600.1:n.203-56428T>C
XM_011535299.1:c.65-56428T>C	XP_011533601.1:n.65-56428T>C
XM_011535299.3:c.65-56428T>C	XP_011533601.1:n.65-56428T>C
XM_017020834.2:c.125-56428T>C	XP_016876323.1:n.125-56428T>C
XM_017020835.2:c.65-56428T>C	XP_016876324.1:n.65-56428T>C
XM_024449429.1:c.65-56428T>C	XP_024305197.1:n.65-56428T>C
NM_178006.4:c.170-56428T>C MANE Select	NP_821074.1:n.170-56428T>C
NM_001243476.3:c.65-56428T>C	NP_001230405.1:n.65-56428T>C