Canonical Allele Identifier: CA1504512193

Gene: TMEM131L

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.153636464C= , CM000666.2:g.153636464C=	GRCh38
NC_000004.11:g.154557616C= , CM000666.1:g.154557616C=	GRCh37
NC_000004.10:g.154777066C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409959.8:c.4721C= MANE Select	ENSP00000386787.3:p.Pro1574=
ENST00000240487.5:c.4052C=	ENSP00000240487.5:p.Pro1351=
ENST00000409663.7:c.4718C=	ENSP00000386574.3:p.Pro1573=
ENST00000409959.7:c.4721C=	ENSP00000386787.3:p.Pro1574=
NM_001131007.1:c.4721C=	NP_001124479.1:p.Pro1574=
NM_015196.3:c.4718C=	NP_056011.3:p.Pro1573=
XM_005262871.3:c.2843C=	XP_005262928.2:p.Pro948=
XM_011531780.1:c.4808C=	XP_011530082.1:p.Pro1603=
XM_011531781.1:c.4805C=	XP_011530083.1:p.Pro1602=
XM_011531782.1:c.4778C=	XP_011530084.1:p.Pro1593=
XM_011531783.1:c.4556C=	XP_011530085.1:p.Pro1519=
XM_017007925.1:c.4718C=	XP_016863414.1:p.Pro1573=
XM_017007926.1:c.4715C=	XP_016863415.1:p.Pro1572=
XM_024453956.1:c.4778C=	XP_024309724.1:p.Pro1593=
XM_024453957.1:c.4775C=	XP_024309725.1:p.Pro1592=
XM_024453958.1:c.2843C=	XP_024309726.1:p.Pro948=
NM_001131007.2:c.4721C= MANE Select	NP_001124479.1:p.Pro1574=
NM_015196.4:c.4718C=	NP_056011.3:p.Pro1573=