Canonical Allele Identifier: CA393235200

Gene: TMEM202

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72407210G>C , CM000677.2:g.72407210G>C	GRCh38
NC_000015.9:g.72699551G>C , CM000677.1:g.72699551G>C	GRCh37
NC_000015.8:g.70486605G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001080462.3:c.612G>C MANE Select	NP_001073931.1:p.Met204Ile
ENST00000341689.4:c.612G>C MANE Select	ENSP00000340212.3:p.Met204Ile
NM_001080462.1:c.612G>C	NP_001073931.1:p.Met204Ile
NM_001080462.2:c.612G>C	NP_001073931.1:p.Met204Ile
NR_148418.1:n.370G>C
NR_148418.2:n.378G>C
NR_148419.1:n.245+459G>C
NR_148419.2:n.253+459G>C
ENST00000341689.3:c.612G>C	ENSP00000340212.3:p.Met204Ile
ENST00000567679.1:c.*45+459G>C	ENSP00000456083.1:n.*45+459G>C
ENST00000568167.5:c.*170G>C	ENSP00000457632.1:n.*170G>C
ENST00000649825.1:c.279G>C	ENSP00000497819.1:p.Met93Ile
XM_011521497.1:c.495G>C	XP_011519799.1:p.Met165Ile
XM_011521497.2:c.495G>C	XP_011519799.1:p.Met165Ile
XM_011521498.1:c.487+459G>C	XP_011519800.1:n.487+459G>C
XM_011521499.1:c.279G>C	XP_011519801.1:p.Met93Ile
XM_011521499.2:c.279G>C	XP_011519801.1:p.Met93Ile
XM_011521500.1:c.279G>C	XP_011519802.1:p.Met93Ile
XM_024449910.1:c.487+459G>C	XP_024305678.1:n.487+459G>C