Canonical Allele Identifier: CA2838426884

Gene: P4HA2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.132195570C>A , CM000667.2:g.132195570C>A	GRCh38
NC_000005.9:g.131531263C>A , CM000667.1:g.131531263C>A	GRCh37
NC_000005.8:g.131559162C>A	NCBI36
NG_052887.1:g.37294G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360568.8:c.1366-90G>T MANE Select	ENSP00000353772.3:n.1366-90G>T
ENST00000379100.7:c.1366-90G>T	ENSP00000368394.2:n.1366-90G>T
ENST00000379104.7:c.1372-90G>T MANE Plus Clinical	ENSP00000368398.2:n.1372-90G>T
ENST00000428369.6:c.*926-90G>T	ENSP00000396495.1:n.*926-90G>T
ENST00000166534.8:c.1372-90G>T	ENSP00000166534.4:n.1372-90G>T
ENST00000360568.7:c.1366-90G>T	ENSP00000353772.3:n.1366-90G>T
ENST00000379086.5:c.1366-90G>T	ENSP00000368379.1:n.1366-90G>T
ENST00000379100.6:c.1366-90G>T	ENSP00000368394.2:n.1366-90G>T
ENST00000379104.6:c.1372-90G>T	ENSP00000368398.2:n.1372-90G>T
ENST00000401867.5:c.1372-90G>T	ENSP00000384999.1:n.1372-90G>T
ENST00000467587.1:n.161G>T
NM_001017973.1:c.1366-90G>T	NP_001017973.1:n.1366-90G>T
NM_001017974.1:c.1366-90G>T	NP_001017974.1:n.1366-90G>T
NM_001142598.1:c.1366-90G>T	NP_001136070.1:n.1366-90G>T
NM_001142599.1:c.1372-90G>T	NP_001136071.1:n.1372-90G>T
NM_004199.2:c.1372-90G>T	NP_004190.1:n.1372-90G>T
XM_005272116.3:c.1372-90G>T	XP_005272173.1:n.1372-90G>T
XM_005272117.3:c.1372-90G>T	XP_005272174.1:n.1372-90G>T
XM_005272118.3:c.1372-90G>T	XP_005272175.1:n.1372-90G>T
XM_005272119.3:c.1372-90G>T	XP_005272176.1:n.1372-90G>T
XM_005272120.3:c.1372-90G>T	XP_005272177.1:n.1372-90G>T
XM_006714728.2:c.1372-90G>T	XP_006714791.1:n.1372-90G>T
XM_006714729.2:c.1366-90G>T	XP_006714792.1:n.1366-90G>T
XM_006714730.2:c.1366-90G>T	XP_006714793.1:n.1366-90G>T
XM_011543705.1:c.1195-90G>T	XP_011542007.1:n.1195-90G>T
NM_001365677.1:c.1372-90G>T	NP_001352606.1:n.1372-90G>T
NM_001365678.1:c.1366-90G>T	NP_001352607.1:n.1366-90G>T
NM_001365679.1:c.1366-90G>T	NP_001352608.1:n.1366-90G>T
NM_001365680.1:c.1366-90G>T	NP_001352609.1:n.1366-90G>T
NM_001365681.1:c.1189-90G>T	NP_001352610.1:n.1189-90G>T
XM_005272117.4:c.1372-90G>T	XP_005272174.1:n.1372-90G>T
XM_005272118.4:c.1372-90G>T	XP_005272175.1:n.1372-90G>T
XM_005272119.4:c.1372-90G>T	XP_005272176.1:n.1372-90G>T
XM_005272120.4:c.1372-90G>T	XP_005272177.1:n.1372-90G>T
XM_006714728.3:c.1372-90G>T	XP_006714791.1:n.1372-90G>T
XM_024446255.1:c.1195-90G>T	XP_024302023.1:n.1195-90G>T
XM_024446256.1:c.1189-90G>T	XP_024302024.1:n.1189-90G>T
NM_001017974.2:c.1366-90G>T MANE Select	NP_001017974.1:n.1366-90G>T
NM_001142598.2:c.1366-90G>T	NP_001136070.1:n.1366-90G>T
NM_001142599.2:c.1372-90G>T	NP_001136071.1:n.1372-90G>T
NM_001365677.2:c.1372-90G>T MANE Plus Clinical	NP_001352606.1:n.1372-90G>T
NM_001365678.2:c.1366-90G>T	NP_001352607.1:n.1366-90G>T
NM_001365679.2:c.1366-90G>T	NP_001352608.1:n.1366-90G>T
NM_001365680.2:c.1366-90G>T	NP_001352609.1:n.1366-90G>T
NM_001365681.2:c.1189-90G>T	NP_001352610.1:n.1189-90G>T
NM_004199.3:c.1372-90G>T	NP_004190.1:n.1372-90G>T