Canonical Allele Identifier: CA1662441704

Gene: THEMIS

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.127873328C= , CM000668.2:g.127873328C=	GRCh38
NC_000006.11:g.128194473C= , CM000668.1:g.128194473C=	GRCh37
NC_000006.10:g.128236166C=	NCBI36
NG_016226.1:g.50304G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368248.5:c.92-18140G= MANE Select	ENSP00000357231.2:n.92-18140G=
ENST00000434358.3:c.92-18140G=	ENSP00000387740.3:n.92-18140G=
ENST00000368248.4:c.92-18140G=	ENSP00000357231.2:n.92-18140G=
ENST00000368250.5:c.92-18140G=	ENSP00000357233.2:n.92-18140G=
ENST00000434358.2:c.118-18140G=
ENST00000537166.5:c.-14-18140G=	ENSP00000439863.1:n.-14-18140G=
ENST00000626040.2:c.-146-18140G=	ENSP00000486494.1:n.-146-18140G=
ENST00000630369.2:c.92-18140G=	ENSP00000487358.1:n.92-18140G=
NM_001010923.2:c.92-18140G=	NP_001010923.1:n.92-18140G=
NM_001164685.1:c.92-18140G=	NP_001158157.1:n.92-18140G=
NM_001164687.1:c.-14-18140G=	NP_001158159.1:n.-14-18140G=
XM_011535813.1:c.92-18140G=	XP_011534115.1:n.92-18140G=
XM_011535814.1:c.-14-18140G=	XP_011534116.1:n.-14-18140G=
XM_011535816.1:c.-423-18140G=	XP_011534118.1:n.-423-18140G=
XM_011535817.1:c.-330-18140G=	XP_011534119.1:n.-330-18140G=
XM_011535814.2:c.-14-18140G=	XP_011534116.1:n.-14-18140G=
XM_017010848.1:c.92-18140G=	XP_016866337.1:n.92-18140G=
XM_017010849.1:c.92-18140G=	XP_016866338.1:n.92-18140G=
XM_024446433.1:c.92-18140G=	XP_024302201.1:n.92-18140G=
XM_024446434.1:c.-576-18140G=	XP_024302202.1:n.-576-18140G=
NM_001164687.2:c.-14-18140G=	NP_001158159.1:n.-14-18140G=
NM_001010923.3:c.92-18140G= MANE Select	NP_001010923.1:n.92-18140G=
NM_001164685.2:c.92-18140G=	NP_001158157.1:n.92-18140G=
NM_001394520.1:c.-14-18140G=	NP_001381449.1:n.-14-18140G=
NM_001394521.1:c.92-18140G=	NP_001381450.1:n.92-18140G=
NM_001394522.1:c.-380-18140G=	NP_001381451.1:n.-380-18140G=