Canonical Allele Identifier: CA7119470

Gene: DHRS4

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23966355C>T , CM000676.2:g.23966355C>T	GRCh38
NC_000014.8:g.24435564C>T , CM000676.1:g.24435564C>T	GRCh37
NC_000014.7:g.23505404C>T	NCBI36
NG_023545.1:g.1482C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_021004.4:c.604C>T MANE Select	NP_066284.2:p.Pro202Ser
ENST00000313250.10:c.604C>T MANE Select	ENSP00000326219.5:p.Pro202Ser
NM_001282987.1:c.460+372C>T	NP_001269916.1:n.460+372C>T
NM_001282987.2:c.460+372C>T	NP_001269916.1:n.460+372C>T
NM_001282988.1:c.502C>T	NP_001269917.1:p.Pro168Ser
NM_001282988.2:c.502C>T	NP_001269917.1:p.Pro168Ser
NM_001282989.1:c.409-856C>T	NP_001269918.1:n.409-856C>T
NM_001282989.2:c.409-856C>T	NP_001269918.1:n.409-856C>T
NM_001282990.1:c.429+372C>T	NP_001269919.1:n.429+372C>T
NM_001282990.2:c.429+372C>T	NP_001269919.1:n.429+372C>T
NM_001282991.1:c.307-856C>T	NP_001269920.1:n.307-856C>T
NM_001282991.2:c.307-856C>T	NP_001269920.1:n.307-856C>T
NM_021004.3:c.604C>T	NP_066284.2:p.Pro202Ser
ENST00000313250.9:c.604C>T	ENSP00000326219.5:p.Pro202Ser
ENST00000397074.7:c.307-856C>T	ENSP00000380264.3:n.307-856C>T
ENST00000397075.7:c.409-856C>T	ENSP00000380265.3:n.409-856C>T
ENST00000543741.6:c.409-856C>T	ENSP00000440508.2:n.409-856C>T
ENST00000558263.5:c.460+372C>T	ENSP00000453367.1:n.460+372C>T
ENST00000558581.5:c.502C>T	ENSP00000452645.1:p.Pro168Ser
ENST00000559632.5:c.429+372C>T	ENSP00000453983.1:n.429+372C>T
XM_006720005.2:c.531+372C>T	XP_006720068.1:n.531+372C>T
XM_006720005.3:c.531+372C>T	XP_006720068.1:n.531+372C>T