Canonical Allele Identifier: CA3611021

Gene: TRIM41

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.181234425C>T , CM000667.2:g.181234425C>T	GRCh38
NC_000005.9:g.180661425C>T , CM000667.1:g.180661425C>T	GRCh37
NC_000005.8:g.180594031C>T	NCBI36
NG_030346.1:g.16163C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_033549.5:c.1543C>T MANE Select	NP_291027.3:p.Pro515Ser
ENST00000315073.10:c.1543C>T MANE Select	ENSP00000320869.5:p.Pro515Ser
NM_033549.4:c.1543C>T	NP_291027.3:p.Pro515Ser
NM_201627.2:c.1467+76C>T	NP_963921.1:n.1467+76C>T
NM_201627.3:c.1467+76C>T	NP_963921.1:n.1467+76C>T
NR_045218.1:n.2181+76C>T
NR_045218.2:n.2163+76C>T
ENST00000315073.9:c.1543C>T	ENSP00000320869.5:p.Pro515Ser
ENST00000351937.9:c.1467+76C>T	ENSP00000336749.6:n.1467+76C>T
ENST00000503114.1:c.1386+76C>T
ENST00000508930.1:n.2453C>T
ENST00000510072.1:n.359C>T
ENST00000514219.1:c.331+76C>T
ENST00000515223.1:n.4329C>T
XM_006714929.2:c.1473+70C>T	XP_006714992.1:n.1473+70C>T
XM_006714930.2:c.1467+76C>T	XP_006714993.1:n.1467+76C>T
XM_006714931.2:c.1463+80C>T	XP_006714994.1:n.1463+80C>T
XM_006714931.3:c.1463+80C>T	XP_006714994.1:n.1463+80C>T
XM_006714932.2:c.1473+70C>T	XP_006714995.1:n.1473+70C>T
XM_006714932.3:c.1473+70C>T	XP_006714995.1:n.1473+70C>T
XR_941119.1:n.2278C>T
XR_941119.2:n.1543C>T